IQVIA Hiring CRA 2 – Clinical Research Associate

Clinical Research Associate Openings - IQVIA

WhatsApp Group Join Now

Telegram Group Join Now

Instagram Group Join Now

Share With Your Friends

WhatsApp Telegram LinkedIn X Facebook Copy Email Pinterest

IQVIA Hiring CRA 2 – Clinical Research Associate Jobs in Thane for Life Sciences Professionals
Company Overview
Job Role and Responsibilities
Clinical Trial Monitoring
Site Management and Study Oversight
Regulatory Documentation and Compliance
Data Management and Reporting
Study Execution and Collaboration
Site Financial Management
Eligibility and Qualifications
Educational Qualification
Experience
Technical Skills
Professional Skills
Location and Salary
Application Process
Frequently Asked Questions
What does a Clinical Research Associate (CRA) do?
Who can apply for the CRA 2 role at IQVIA?
What is GCP in clinical research?
Is travel required for a CRA role?
Where is the job located?
Job Summary

Full Time
Mumbai
Posted 7 hours ago

IQVIA

IQVIA Hiring CRA 2 – Clinical Research Associate Jobs in Thane for Life Sciences Professionals

IQVIA is currently recruiting for the position of Clinical Research Associate II (CRA 2) in Thane, India. This is a full‑time field‑based clinical research role designed for professionals with experience in clinical trial monitoring, site management, and regulatory compliance. The vacancy is part of IQVIA’s global clinical operations team and focuses on ensuring that clinical trials are conducted according to approved protocols, regulatory standards, and sponsor requirements.

Candidates with a Bachelor’s degree in life sciences, pharmacy, nursing, or healthcare disciplines and at least one year of on‑site monitoring experience are encouraged to apply. The role offers the opportunity to work directly with research sites, investigators, and global clinical development teams while supporting the advancement of innovative therapies and medical treatments.

This position provides strong career growth for professionals seeking to build long‑term careers in clinical research, clinical trial monitoring, and global CRO operations.

Company Overview

IQVIA is one of the world’s leading clinical research organizations (CROs) providing advanced analytics, clinical development services, and healthcare intelligence to pharmaceutical, biotechnology, and medical device companies. The organization combines clinical research expertise with real‑world data analytics and technology platforms to accelerate drug development and improve healthcare outcomes.

Operating in more than 100 countries, IQVIA collaborates with pharmaceutical sponsors, healthcare institutions, and regulatory bodies to support clinical trials across a wide range of therapeutic areas including oncology, cardiology, infectious diseases, and neurology.

Through its integrated approach to clinical research, real‑world evidence, and commercial analytics, IQVIA helps bring innovative medicines to patients faster while ensuring compliance with international regulatory standards.

Employees working at IQVIA gain exposure to multinational clinical trials, cutting‑edge research technologies, and global healthcare data systems that support evidence‑based medicine and improved patient outcomes.

Job Role and Responsibilities

The Clinical Research Associate II (CRA 2) is responsible for performing site monitoring and site management activities to ensure that clinical trials are conducted according to the approved study protocol, regulatory guidelines, and sponsor expectations.

This role requires strong knowledge of clinical trial processes, regulatory compliance, and site monitoring practices used in pharmaceutical research.

Clinical Trial Monitoring

• Conduct site monitoring visits including site selection, site initiation, monitoring visits, and site close‑out activities

• Ensure clinical research sites conduct studies in compliance with Good Clinical Practice (GCP) and ICH guidelines

• Verify that study data is accurately collected, documented, and reported according to the study protocol

• Monitor site performance and adherence to regulatory requirements

Site Management and Study Oversight

• Establish effective communication with investigators and site staff

• Provide protocol training and guidance to clinical research sites

• Monitor patient recruitment and enrollment progress

• Support site teams in meeting subject recruitment targets

• Address site issues and escalate quality concerns where required

Regulatory Documentation and Compliance

• Track regulatory submissions, approvals, and essential study documentation

• Ensure site documents are properly maintained in the Trial Master File (TMF)

• Verify that the Investigator Site File (ISF) complies with GCP and regulatory requirements

• Maintain accurate documentation of monitoring visit findings and action plans

Data Management and Reporting

• Track completion and submission of Case Report Forms (CRFs)

• Monitor query generation and resolution within clinical data systems

• Submit monitoring visit reports and follow‑up letters after site visits

• Ensure accurate documentation of monitoring activities and site communications

Study Execution and Collaboration

• Collaborate with project managers, clinical operations teams, and sponsors

• Support study start‑up activities when required

• Assist with development of subject recruitment strategies for research sites

• Coordinate with project teams to ensure timely study progress

Site Financial Management

• Support management of site payments according to the clinical trial agreement

• Assist with retrieval and review of site invoices when applicable

• Ensure financial documentation aligns with study contracts and project budgets

Through these responsibilities, the CRA 2 role ensures the quality, integrity, and regulatory compliance of clinical trials, which is critical for bringing safe and effective medicines to patients worldwide.

Eligibility and Qualifications

Candidates applying for the Clinical Research Associate II role should possess academic qualifications in healthcare or life sciences along with relevant clinical research experience.

Educational Qualification

Bachelor’s degree in scientific or healthcare disciplines.

Relevant educational backgrounds include:

BPharmacy, MPharmacy, BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Nursing, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Clinical Research, MSc Life Sciences, PharmD.

Experience

• Minimum 1 year of on‑site clinical trial monitoring experience as a Clinical Research Associate or equivalent role

• Experience working within clinical research organizations (CROs), pharmaceutical companies, or healthcare research institutions is preferred

Technical Skills

• Knowledge of Good Clinical Practice (GCP) guidelines

• Understanding of ICH clinical research regulations

• Experience with clinical trial monitoring and site management

• Familiarity with Trial Master File (TMF) documentation systems

• Knowledge of clinical trial documentation and case report form processes

• Proficiency in Microsoft Office tools including Word, Excel, and PowerPoint

Professional Skills

• Strong communication and interpersonal skills

• Excellent organizational and time management abilities

• Problem‑solving and analytical skills

• Ability to build effective working relationships with investigators and project teams

• Ability to manage multiple clinical sites and project timelines

Professionals with experience in clinical monitoring, clinical trial site management, regulatory compliance, and pharmaceutical research operations will find this role highly aligned with career advancement in global clinical research organizations.

Location and Salary

Location: Thane, Maharashtra, India

Work Type: Field‑based clinical research role

Employment Type: Full‑time

Salary: Competitive salary package aligned with global CRO industry standards and candidate experience.

Employees at IQVIA gain access to global clinical development projects, professional training programs, and opportunities to work with leading pharmaceutical sponsors worldwide.

Application Process

Candidates interested in applying for the Clinical Research Associate II (CRA 2) role can submit their applications through the official IQVIA careers portal.

Apply Here:

https://jobs.iqvia.com/en/jobs/R1527417-0

Applicants are encouraged to apply early since clinical research associate roles in global CRO organizations often receive a high volume of qualified applications.

Frequently Asked Questions

What does a Clinical Research Associate (CRA) do?

A Clinical Research Associate monitors clinical trial sites to ensure studies are conducted according to protocol, regulatory guidelines, and ethical standards. CRAs verify study data accuracy and support investigators throughout the clinical trial process.

Who can apply for the CRA 2 role at IQVIA?

Candidates with a bachelor’s degree in life sciences, pharmacy, nursing, biotechnology, or clinical research with at least one year of clinical trial monitoring experience can apply.

What is GCP in clinical research?

Good Clinical Practice (GCP) is an international ethical and scientific quality standard used for designing, conducting, monitoring, and reporting clinical trials involving human participants.

Is travel required for a CRA role?

Yes. Clinical Research Associates typically travel to research sites to conduct monitoring visits and ensure study compliance.

Where is the job located?

The role is based in Thane, India, and involves field‑based monitoring activities across clinical research sites.

Job Summary

Category	Details
Company	IQVIA
Vacancies	Clinical Research Associate II (CRA 2)
Required Education	BPharmacy, MPharmacy, BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Nursing, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Clinical Research, MSc Life Sciences, PharmD
Experience	Minimum 1 year Clinical Trial Monitoring Experience

Tagged as: Pharma Jobs in Mumbai

Join whatsaapp: Join whatsapp Channel

Share With Your Friends

WhatsApp Telegram LinkedIn X Facebook Copy Email Pinterest

Upcoming Walkins🚶

Bharat Biotech walk‑in Production – Bioprocess / Formulation & Filling

March 11, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Bharat Biotech Production Jobs ITI Diploma Hyderabad ITI, Diploma, Graduation, PG candidates with 3–10 yrs experience can attend Bharat Biotech Production walk‑in interview at Hyderabad. Bharat Biotech International Ltd., one of India’s most recognized biotechnology companies, has announced a walk‑in interview for experienced professionals in vaccine and injectable manufacturing. The company is currently hiring skilled candidates for Production roles in Drug Substance (Bioprocess) and Drug Product (Formulation & Filling) at its state‑of‑the‑art facility located in Genome Valley, Hyderabad. This recruitment drive is designed for candidates with 3–10 years of experience in injectable or vaccine manufacturing environments who hold qualifications such as ITI, Diploma, Graduation, or Post‑Graduation in relevant life sciences or engineering disciplines. The walk‑in interview will take place on 14th March 2026. Professionals working in vaccine manufacturing play a crucial role in the global healthcare ecosystem. From cell culture development and fermentation processes to purification and sterile filling operations, production specialists ensure that vaccines and biologics are manufactured safely, efficiently, and in compliance with international regulatory guidelines. Bharat Biotech is seeking candidates with experience in bioprocess manufacturing, upstream processing, downstream purification, sterile formulation, aseptic filling, isolator technology, and vaccine production operations. These professionals will contribute directly to the company’s mission of developing life‑saving vaccines and biotechnology products that protect millions of people worldwide. For candidates aiming to advance their careers in biotechnology manufacturing, vaccine production, and biopharmaceutical processing, this opportunity provides exposure to advanced vaccine production technologies and internationally compliant manufacturing systems. Company Overview Bharat Biotech International Limited is a globally recognized biotechnology company headquartered in Hyderabad, India. The organization is known for developing innovative vaccines and biopharmaceutical products that address major global health challenges. Founded with a vision to deliver affordable and high‑quality vaccines, Bharat Biotech has become a key contributor to global immunization programs. The company has developed several widely used vaccines and biotherapeutic products distributed across multiple international markets. Bharat Biotech operates advanced manufacturing facilities designed specifically for biotechnology research, vaccine production, and biologics manufacturing. These facilities follow strict regulatory standards established by global regulatory authorities including: • WHO (World Health Organization) • USFDA (United States Food and Drug Administration) • EMA (European Medicines Agency) • CDSCO (Central Drugs Standard Control Organization) The company’s flagship campus in Genome Valley, Hyderabad is one of India’s largest biotechnology clusters. This region hosts numerous pharmaceutical, biotechnology, and vaccine research companies and has become a major hub for biotechnology innovation. Bharat Biotech focuses on several areas including: • Vaccine research and development • Biopharmaceutical manufacturing • Viral vaccine production • Recombinant biotechnology products • Clinical research and global regulatory approvals Professionals joining Bharat Biotech gain exposure to cutting‑edge technologies in bioprocess engineering, vaccine fermentation, sterile injectable manufacturing, downstream purification, and GMP‑compliant biotechnology production systems. Job Role & Responsibilities The company is hiring experienced professionals for Production roles in both Drug Substance and Drug Product manufacturing divisions. Drug Substance – Bioprocess Manufacturing Drug substance manufacturing involves producing the active biological component used in vaccines and biologic medicines. Key responsibilities include: • Performing upstream bioprocess operations including cell culture and fermentation • Monitoring bioreactors and fermentation systems • Ensuring sterile handling of biological materials • Maintaining bioprocess documentation according to GMP guidelines These activities help ensure the consistency and quality of biological drug substances. Upstream Processing Operations Upstream processing focuses on growing biological cells used to produce vaccines and biologic products. Key responsibilities include: • Operating cell culture systems • Managing fermentation processes • Monitoring environmental and process parameters • Supporting autoclave operations for sterilization These processes form the foundation of biologics manufacturing. Downstream Processing Operations Downstream processing focuses on purification and recovery of biological products after fermentation. Key responsibilities include: • Performing virus culture operations • Handling centrifugation and filtration processes • Conducting purification and chromatography procedures • Supporting Tangential Flow Filtration (TFF) operations These purification processes ensure that vaccine components meet strict quality specifications. Drug Product – Formulation & Filling Drug product manufacturing involves converting purified biological substances into final vaccine formulations. Key responsibilities include: • Preparing sterile formulations • Operating aseptic filling systems for vials, BFS, and PFS • Handling isolators and restricted access barrier systems (RABS) • Performing vial washing and sterilization processes These processes ensure the safe packaging of vaccines for distribution. Sealing, Capping, and Packaging Operations Final production stages involve sealing vaccine containers and preparing them for distribution. Key responsibilities include: • Performing vial sealing and capping operations • Supporting packaging and labeling procedures • Ensuring batch documentation is completed accurately These steps ensure product traceability and regulatory compliance. Eligibility / Qualifications Bharat Biotech is inviting applications from experienced candidates with biotechnology or pharmaceutical manufacturing backgrounds. Required Educational Qualifications ITI, Diploma, Graduation, Post‑Graduation Relevant disciplines include: Biotechnology, Microbiology, Biochemistry, Life Sciences, Pharmacy, Chemical Engineering, Mechanical Engineering These educational programs provide knowledge related to biotechnology manufacturing processes, fermentation science, pharmaceutical production systems, and laboratory techniques. Experience Requirement Candidates must have 3 to 10 years of experience in injectable or vaccine manufacturing environments. Relevant experience includes: • Bioprocess manufacturing • Vaccine production operations • Sterile injectable manufacturing • Fermentation and cell culture systems • Biopharmaceutical purification processes Candidates must be willing to work in shift‑based manufacturing operations. Required Skills Ideal candidates should demonstrate: • Knowledge of vaccine manufacturing processes • Experience in aseptic manufacturing environments • Understanding of GMP and biotechnology regulatory guidelines • Strong documentation and process monitoring skills • Ability to work in controlled manufacturing environments Professionals experienced in biologics manufacturing, fermentation technology, or sterile injectable production will have a strong advantage. Location & Salary Job Location Bharat Biotech International Ltd Genome Valley, Turkapally, Shamirpet Hyderabad, Telangana Genome Valley is India’s leading biotechnology hub hosting numerous global pharmaceutical and biotechnology companies. Salary Salary packages are determined based on candidate experience, skill level, and company policies. Biotechnology production professionals typically receive competitive compensation along with long‑term career growth opportunities. Application Process Interested candidates can attend the walk‑in interview scheduled by Bharat Biotech. Interview Details: Date: 14 March 2026 (Saturday) Time: 10:00 AM – 03:00 PM Venue: Bharat Biotech International Ltd. Genome Valley, Turkapally, Shamirpet Hyderabad, Telangana Candidates must carry the following documents: • Updated resume • Aadhaar card • PAN card • Passport‑size photographs Candidates will be evaluated based on their technical experience, manufacturing knowledge, and regulatory compliance understanding. Why Build a Career in Vaccine Manufacturing Vaccine manufacturing is one of the most critical areas in modern biotechnology and global healthcare. Professionals working in this field contribute directly to the development and distribution of vaccines that protect populations from infectious diseases. Biotechnology manufacturing professionals gain expertise in: • Bioprocess engineering • Fermentation technology • Biopharmaceutical purification • Sterile injectable manufacturing • Global biotechnology regulatory compliance These skills are highly valuable across industries including: • Vaccine manufacturing companies • Biopharmaceutical companies • Biotechnology research organizations • Global pharmaceutical manufacturers Career growth opportunities in this field include: • Bioprocess Engineer • Vaccine Manufacturing Specialist • Biopharmaceutical Production Manager • Biotechnology Operations Manager Professionals working in vaccine manufacturing contribute significantly to global healthcare advancement by supporting the production of life‑saving vaccines and biologic therapies. Frequently Asked Questions (FAQs) Who can attend the Bharat Biotech walk‑in interview? Candidates with ITI, Diploma, Graduation, or Post‑Graduation qualifications and 3–10 years of experience in injectable or vaccine manufacturing can attend. Which departments are hiring? The recruitment is for Production roles in Drug Substance (Bioprocess) and Drug Product (Formulation & Filling). Where is the interview location? The interview will be conducted at Bharat Biotech’s Genome Valley facility in Hyderabad. What experience is required? Candidates should have experience in biologics manufacturing, vaccine production, or sterile injectable production. What documents should candidates bring? Candidates must bring their updated resume, Aadhaar card, PAN card, and passport‑size photos. Job Summary Company Bharat Biotech International Ltd Vacancies Production – Bioprocess / Formulation & Filling Required Education ITI, Diploma, Graduation, Post‑Graduation Experience 3 – 10 Years [...] Read more...

Axis walk‑in Bioanalytical & Medical Writing

March 11, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BPharm MPharm Fresher Jobs | Axis Clinicals Hyderabad BPharm, MPharm, PharmD fresher vacancies at Axis Clinicals Hyderabad for Bioanalytical & Medical Writing roles. Axis Clinicals Limited has announced a walk‑in recruitment drive for fresh graduates interested in starting their careers in clinical research, bioanalytical sciences, pharmacokinetics, biostatistics, and medical writing. The walk‑in drive will take place at the company’s Hyderabad location and is open to 2023, 2024, and 2025 pass‑out candidates who want to enter the rapidly growing pharmaceutical and clinical research industry. Clinical research organizations (CROs) play a vital role in drug development by supporting pharmaceutical companies with clinical trials, bioanalytical testing, pharmacokinetic analysis, regulatory documentation, and scientific medical writing. Professionals working in these areas contribute directly to the development of safe and effective medicines used worldwide. Axis Clinicals is inviting candidates with B.Pharm, M.Pharm, and Pharm.D qualifications to join its organization as Trainee Research Associates in departments such as Bioanalytical Research, Pharmacokinetics & Biostatistics, and Medical Writing. This opportunity allows fresh graduates to gain hands‑on exposure to clinical trial research, regulatory documentation, pharmacokinetic data analysis, and scientific report preparation. Working at a clinical research organization offers a unique career path where professionals gain experience in drug development processes, regulatory compliance, clinical data management, and scientific communication. For fresh graduates interested in pharmaceutical research and development, this recruitment drive represents an excellent starting point for a long‑term career in the life sciences industry. Company Overview Axis Clinicals Limited is a well‑established clinical research organization headquartered in Hyderabad, India. The company specializes in providing comprehensive clinical research and bioanalytical services to pharmaceutical, biotechnology, and healthcare organizations globally. Clinical research organizations support pharmaceutical companies during various stages of drug development, including clinical trials, bioequivalence studies, pharmacokinetic evaluations, and regulatory documentation. Axis Clinicals has developed strong expertise in conducting high‑quality clinical studies that comply with international regulatory standards. The company offers a range of specialized services including: • Bioanalytical laboratory testing • Clinical trial management • Pharmacokinetic and biostatistical analysis • Medical and regulatory writing • Clinical data management Axis Clinicals operates advanced clinical research facilities equipped with modern analytical technologies and specialized laboratories that support pharmaceutical drug development activities. The organization follows globally recognized regulatory standards such as: • ICH‑GCP (International Council for Harmonisation – Good Clinical Practice) • USFDA clinical research guidelines • CDSCO clinical trial regulations • GLP (Good Laboratory Practices) Through its experienced scientific teams and advanced research infrastructure, Axis Clinicals contributes to the development of new medicines and therapies that improve patient health outcomes worldwide. Employees joining Axis Clinicals gain valuable exposure to clinical trial research operations, pharmaceutical regulatory systems, scientific documentation practices, and global clinical research standards. Job Role & Responsibilities Axis Clinicals is hiring fresh graduates for multiple trainee positions in clinical research departments. Selected candidates will receive structured training and hands‑on experience in specialized research functions. Trainee Research Associate – Bioanalytical Bioanalytical research associates work in laboratory environments responsible for analyzing biological samples collected during clinical trials. Key responsibilities include: • Performing bioanalytical testing of clinical samples • Supporting sample preparation and analytical procedures • Operating analytical instruments used in bioanalysis • Maintaining laboratory documentation according to GLP guidelines • Supporting method development and validation activities Bioanalytical scientists play a crucial role in determining how drugs behave in the human body during clinical trials. Trainee Research Associate – Pharmacokinetics & Biostatistics Pharmacokinetics and biostatistics professionals analyze clinical trial data to understand drug absorption, distribution, metabolism, and elimination. Key responsibilities include: • Assisting in pharmacokinetic data analysis • Supporting statistical evaluation of clinical trial results • Preparing pharmacokinetic study reports • Maintaining clinical research documentation • Collaborating with clinical research teams during data interpretation These activities help researchers evaluate the safety and effectiveness of pharmaceutical products during clinical trials. Trainee Research Associate – Medical Writing Medical writers are responsible for preparing scientific and regulatory documents required during drug development and clinical trials. Key responsibilities include: • Preparing clinical study reports and regulatory documents • Writing scientific summaries and research documentation • Reviewing clinical data for accuracy and clarity • Supporting preparation of regulatory submission documents • Ensuring compliance with regulatory writing guidelines Medical writing professionals ensure that clinical research findings are communicated clearly and accurately to regulatory authorities and scientific audiences. Eligibility / Qualifications Axis Clinicals is inviting fresh graduates with pharmaceutical and healthcare educational backgrounds to participate in the walk‑in drive. Required Educational Qualifications B.Pharm, M.Pharm (Bioanalytical specialization), M.Pharm (Pharmacology), Pharm.D Relevant academic disciplines include: Pharmacy, Clinical Research, Pharmacology, Pharmaceutical Sciences, Bioanalytical Sciences, Biotechnology, Life Sciences These programs provide foundational knowledge in drug development processes, pharmacokinetics, bioanalysis, clinical research methodologies, and pharmaceutical regulatory standards. Pass‑Out Year Eligibility Candidates must belong to the following graduating batches: • 2023 • 2024 • 2025 Additional Requirements • Candidates must be willing to commit to a two‑year employment agreement. • Candidates who have attended an Axis Clinicals interview in the last six months are not eligible for this drive. Required Skills Ideal candidates should possess: • Strong understanding of pharmaceutical sciences • Basic knowledge of clinical research processes • Scientific writing and documentation abilities • Analytical and data interpretation skills • Attention to detail and accuracy Candidates interested in clinical research careers, bioanalytical laboratories, pharmacokinetic analysis, or regulatory medical writing will benefit greatly from this opportunity. Location & Salary Job Location Axis Clinicals Limited Miyapur, Hyderabad Hyderabad is one of India’s largest pharmaceutical and biotechnology hubs, hosting several global pharmaceutical companies, contract research organizations, and biotechnology research centers. Salary Compensation packages for trainee roles are determined based on company policies, candidate qualifications, and performance during the interview process. Entry‑level roles in clinical research organizations typically include structured training programs and career development opportunities. Application Process Eligible candidates can attend the walk‑in interview directly at the Axis Clinicals facility in Hyderabad. Walk‑In Interview Details Company: Axis Clinicals Limited Location: Miyapur, Hyderabad Dates: 11th March 2026 and 12th March 2026 Time: 9:30 AM – 12:00 PM Candidates attending the interview should bring: • Updated resume • Academic certificates • Government ID proof • Passport size photographs Applicants should arrive early and be prepared for technical and HR interview rounds conducted during the walk‑in recruitment drive. Why Start Your Career in Clinical Research Clinical research is one of the fastest‑growing sectors within the pharmaceutical and biotechnology industries. As new medicines continue to be developed, the demand for trained professionals in clinical trials, bioanalytical research, pharmacokinetic analysis, and medical writing continues to increase. Professionals working in clinical research gain expertise in areas such as: • Drug development processes • Clinical trial documentation and compliance • Bioanalytical laboratory techniques • Pharmacokinetic modeling and statistical analysis • Scientific and regulatory medical writing These skills are highly valued across pharmaceutical companies, contract research organizations (CROs), biotechnology firms, and regulatory consulting companies. Career growth opportunities include: • Clinical Research Associate • Bioanalytical Scientist • Medical Writer • Clinical Data Analyst • Clinical Project Manager Working in clinical research allows professionals to contribute directly to the development of new therapies that improve global healthcare outcomes. Frequently Asked Questions (FAQs) Who can attend the Axis Clinicals walk‑in drive? Fresh graduates from the 2023, 2024, and 2025 batches with B.Pharm, M.Pharm, or Pharm.D qualifications can attend. What positions are available? The company is hiring for Trainee Research Associate roles in Bioanalytical, Pharmacokinetics & Biostatistics, and Medical Writing departments. Is prior experience required? No. These positions are specifically designed for fresh graduates entering the clinical research industry. Where is the interview venue located? The walk‑in interview will take place at the Axis Clinicals office in Miyapur, Hyderabad. Is there any employment commitment? Yes. Selected candidates are expected to commit to a two‑year employment agreement with the company. Job Summary Company Axis Clinicals Limited Vacancies Trainee Research Associate – Bioanalytical, Pharmacokinetics, Medical Writing Required Education B.Pharm, M.Pharm, Pharm.D Experience Freshers (2023–2025 Passouts) [...] Read more...

Lupin Walk‑In Production, QA & QC

March 10, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Lupin API Fresher Walk‑In | BSc MSc Jobs Tarapur BSc, MSc Chemistry fresher vacancies at Lupin Tarapur for Production, QA & QC. 2024‑2025 passouts eligible. Lupin Limited, one of India’s leading pharmaceutical companies with a strong global footprint, has announced a walk‑in recruitment drive for fresh graduates at its API manufacturing facility located in Tarapur, Maharashtra. The company is inviting talented B.Sc, M.Sc Chemistry, and Diploma in Chemical Engineering freshers who are interested in building a long‑term career in Active Pharmaceutical Ingredient (API) manufacturing, pharmaceutical quality control laboratories, and pharmaceutical quality assurance systems. This recruitment initiative is specifically designed for 2024 and 2025 pass‑out candidates who want to start their professional journey in the pharmaceutical industry. Fresh graduates selected through this drive will gain exposure to API production processes, analytical testing laboratories, GMP documentation practices, pharmaceutical process safety, and regulatory compliant manufacturing environments. The pharmaceutical industry requires technically trained professionals who can ensure medicines are manufactured safely, efficiently, and according to strict international regulatory standards. Roles in Production, Quality Control, and Quality Assurance are essential to maintaining the quality and reliability of pharmaceutical products supplied to patients worldwide. Working with a globally recognized pharmaceutical company like Lupin offers fresh graduates a strong foundation in pharmaceutical manufacturing technologies, laboratory analytical systems, regulatory quality standards, and industrial chemical process operations. For candidates seeking stability, skill development, and career progression in the pharmaceutical sector, this walk‑in drive represents a valuable opportunity. Company Overview Lupin Limited is a globally recognized pharmaceutical company headquartered in Mumbai, India. The organization has established itself as a major player in the pharmaceutical industry through its focus on high‑quality medicines, innovative drug development, and large‑scale pharmaceutical manufacturing capabilities. Lupin operates multiple manufacturing facilities across India and internationally, producing Active Pharmaceutical Ingredients (APIs), generic medicines, specialty formulations, and complex pharmaceutical products. The company supplies medicines to more than 100 countries and maintains regulatory approvals from leading global agencies. Lupin manufacturing facilities comply with several international regulatory frameworks including: • USFDA (United States Food and Drug Administration) • EU‑GMP (European Union Good Manufacturing Practices) • WHO‑GMP • MHRA (United Kingdom Medicines and Healthcare Products Regulatory Agency) The Tarapur manufacturing facility in Maharashtra is one of Lupin’s key production sites supporting API manufacturing operations. This plant utilizes modern chemical synthesis processes, advanced quality laboratories, and stringent pharmaceutical quality systems to ensure regulatory compliance and product safety. The company has also been recognized as a Great Place to Work certified organization, demonstrating its commitment to employee welfare, skill development, and professional growth. Fresh graduates joining Lupin will gain hands‑on exposure to pharmaceutical process chemistry, industrial chemical manufacturing, pharmaceutical analytical testing, regulatory compliance systems, and global pharmaceutical quality standards. Job Role & Responsibilities Lupin is hiring fresh graduates for three major departments within its API manufacturing operations: Production (API), Quality Control (QC), and Quality Assurance (QA). Production – API Manufacturing Production professionals are responsible for carrying out chemical manufacturing operations used to produce Active Pharmaceutical Ingredients. Key responsibilities include: • Assisting in API manufacturing processes based on approved batch manufacturing procedures • Monitoring chemical reaction processes during pharmaceutical production • Supporting reactor operations and chemical synthesis activities • Maintaining manufacturing records and batch documentation • Ensuring adherence to Good Manufacturing Practices (GMP) • Supporting plant safety and process control measures Production teams ensure that pharmaceutical APIs are manufactured efficiently while maintaining strict safety and regulatory standards. Quality Control – Analytical Laboratory Quality Control laboratories are responsible for testing raw materials, intermediates, and finished pharmaceutical products to verify their quality. Key responsibilities include: • Performing analytical testing of raw materials and API samples • Operating analytical laboratory instruments • Recording and reviewing laboratory test results • Supporting analytical method validation activities • Maintaining laboratory documentation according to GLP standards Quality Control professionals ensure that pharmaceutical products meet strict quality and purity standards before being approved for release. Quality Assurance – Pharmaceutical Compliance Quality Assurance professionals oversee manufacturing processes to ensure compliance with pharmaceutical regulatory requirements. Key responsibilities include: • Reviewing batch manufacturing records and documentation • Monitoring compliance with Good Manufacturing Practices • Supporting internal quality audits • Ensuring adherence to standard operating procedures (SOPs) • Supporting deviation management and CAPA systems Quality Assurance departments play a vital role in maintaining product quality and regulatory compliance across pharmaceutical manufacturing operations. Eligibility / Qualifications Lupin is inviting fresh graduates who have completed relevant science and technical programs required for pharmaceutical manufacturing roles. Required Educational Qualifications B.Sc Chemistry, M.Sc Chemistry, Diploma in Chemical Engineering These educational programs provide foundational knowledge in industrial chemistry, pharmaceutical manufacturing processes, chemical analysis, and laboratory analytical techniques. Pass‑Out Year Criteria Candidates must have graduated in: • 2024 • 2025 Only freshers are eligible for this walk‑in recruitment drive. Academic Requirement Candidates should have completed their qualification with first‑class academic performance. Required Skills Ideal candidates should demonstrate: • Basic knowledge of pharmaceutical manufacturing concepts • Understanding of chemical process operations • Awareness of GMP guidelines • Strong analytical and problem‑solving skills • Ability to work in industrial manufacturing environments Candidates with academic exposure to industrial chemistry laboratories, pharmaceutical manufacturing processes, or analytical chemistry techniques will have an advantage. Location & Salary Job Location Lupin Ltd T‑142 MIDC Industrial Area Tarapur Via Boisar Tarapur – 401506 Maharashtra Tarapur is a well‑known pharmaceutical and chemical manufacturing hub that hosts several API manufacturing facilities. Salary Salary packages for fresh graduates will be determined based on company policies, academic qualifications, and candidate performance during the interview process. Lupin also offers additional employee benefits including: • Subsidized travel • Food facility • Accommodation support for bachelor employees These benefits make the opportunity especially attractive for candidates relocating for their first professional role. Application Process Eligible candidates can attend the walk‑in interview directly at the Lupin manufacturing facility. Walk‑In Interview Details Date: 11 March 2026 Day: Wednesday Time: 10:30 AM – 2:00 PM Venue: Lupin Ltd, Tarapur T‑142 MIDC Industrial Area Tarapur Via Boisar Tarapur – 401506 Maharashtra Candidates are advised to carry the following documents: • Updated resume • Academic certificates and mark sheets • Government ID proof • Passport size photographs Candidates may also send their resumes in advance to the recruitment team. Email IDs: janmeshktare@lupin.com prachipatil@lupin.com Contact Number for Queries: 7391040115 Shortlisted candidates may be selected after technical and HR evaluation during the walk‑in drive. Why Start Your Pharmaceutical Career with Lupin Starting a career with a globally recognized pharmaceutical company provides fresh graduates with valuable industry exposure. Lupin offers structured learning environments where employees develop practical knowledge in pharmaceutical manufacturing operations, regulatory compliance frameworks, laboratory analytical techniques, and industrial process safety. Professionals working in API manufacturing facilities gain expertise in areas such as: • Chemical synthesis and process chemistry • Pharmaceutical GMP compliance • Analytical chemistry and laboratory testing • Pharmaceutical documentation systems • Industrial safety and process control These skills are highly valued across pharmaceutical companies, biotechnology organizations, and chemical manufacturing industries. Typical career progression in pharmaceutical manufacturing may include: • Production Executive • Quality Control Analyst • Quality Assurance Officer • Manufacturing Supervisor • Pharmaceutical Operations Manager The global pharmaceutical market continues to expand, creating strong demand for technically trained professionals capable of supporting drug manufacturing and quality systems. Frequently Asked Questions (FAQs) Who can attend the Lupin walk‑in interview? Fresh graduates with B.Sc Chemistry, M.Sc Chemistry, or Diploma in Chemical Engineering qualifications can attend. What departments are hiring? The recruitment drive is for Production (API), Quality Control, and Quality Assurance departments. Are experienced candidates eligible? No. This drive is specifically for fresh graduates from the 2024 and 2025 batches. Where is the job location? The position is based at Lupin’s API manufacturing facility in Tarapur, Maharashtra. How can candidates apply? Candidates can either attend the walk‑in interview directly or email their resume to the HR team before the interview date. Job Summary Company Lupin Limited Vacancies API Production Trainee, Quality Control Analyst, Quality Assurance Executive Required Education B.Sc Chemistry, M.Sc Chemistry, Diploma Chemical Experience Freshers (2024–2025 Passouts) [...] Read more...

Emcure Walk‑In Production, QC & Packing

March 10, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Emcure Pharma Injectables Walk‑In | BPharm Jobs Sanand BPharm, MPharm, BSc pharma vacancies at Emcure Pharmaceuticals Sanand for Production, QC & Packing roles. 0‑6 yrs experience. Emcure Pharmaceuticals Ltd., one of India’s leading pharmaceutical companies with strong global regulatory presence, has announced a walk‑in interview drive for multiple pharmaceutical manufacturing roles at its Injectable facility located in Sanand, Ahmedabad, Gujarat. The company is inviting skilled candidates for Production, Quality Control (QC), and Packing departments who want to grow their careers in sterile injectable manufacturing, pharmaceutical quality control laboratories, and GMP‑compliant pharmaceutical operations. Pharmaceutical injectable manufacturing is among the most highly regulated areas within the life sciences industry. Every injectable medicine must be produced in sterile conditions and undergo strict analytical testing to ensure safety, efficacy, and regulatory compliance. Professionals working in injectable facilities gain valuable exposure to sterile pharmaceutical production processes, GMP documentation systems, analytical laboratory testing technologies, and regulatory inspection readiness. Through this walk‑in hiring initiative, Emcure Pharmaceuticals is offering excellent opportunities for candidates with qualifications such as M.Pharm, B.Pharm, B.Sc, M.Sc, Diploma, and ITI who possess experience or interest in pharmaceutical manufacturing operations. Candidates selected through this drive will work in advanced pharmaceutical manufacturing environments supporting complex injectable formulations, sterile production lines, analytical testing laboratories, and packaging operations. For professionals aiming to establish long‑term careers in the pharmaceutical sector, working at Emcure provides exposure to global pharmaceutical quality systems, advanced sterile manufacturing technologies, and regulatory‑compliant pharmaceutical production processes. Company Overview Emcure Pharmaceuticals Ltd. is a globally recognized pharmaceutical company headquartered in Pune, India. The organization focuses on research‑driven pharmaceutical development and manufacturing across a wide range of therapeutic areas. Emcure has built a strong reputation for delivering high‑quality medicines to patients across more than 70 countries. The company operates multiple state‑of‑the‑art pharmaceutical manufacturing facilities that meet international regulatory standards including: • USFDA • EU‑GMP • WHO‑GMP • MHRA • TGA Emcure specializes in manufacturing complex injectable formulations, oral solid dosage forms, biologics, and specialty pharmaceutical products. These facilities are equipped with advanced sterile filling lines, isolator technology, automated packaging systems, and high‑precision analytical laboratories. The Sanand manufacturing facility plays a key role in the company’s global injectable manufacturing operations. Professionals working at this site gain experience in sterile manufacturing technologies, pharmaceutical batch production processes, regulatory documentation systems, and advanced pharmaceutical analytical testing. By maintaining strict adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and global pharmaceutical regulatory frameworks, Emcure ensures the consistent quality and safety of its pharmaceutical products. Employees joining Emcure benefit from working in an environment that emphasizes technical expertise, regulatory compliance, continuous learning, and career advancement within the pharmaceutical industry. Job Role & Responsibilities Emcure Pharmaceuticals is recruiting candidates across three critical departments responsible for pharmaceutical product manufacturing, testing, and packaging. Production Department – Injectable Manufacturing Production professionals working in sterile injectable facilities are responsible for executing batch manufacturing processes while maintaining strict contamination control. Key responsibilities include: • Performing batch manufacturing operations according to approved manufacturing procedures • Handling sterile injectable manufacturing equipment such as filling machines and autoclaves • Monitoring production parameters to ensure batch consistency • Executing leak testing and skid operations • Supporting vial filling and sealing operations • Operating isolator‑based filling systems and VHP sterilization processes Production teams ensure pharmaceutical batches are manufactured safely while maintaining compliance with GMP guidelines and sterile manufacturing protocols. Quality Control Department Quality Control laboratories verify the quality, safety, and potency of pharmaceutical products before they reach patients. Key responsibilities include: • Performing analytical testing of finished products, raw materials, and in‑process samples • Operating analytical instruments such as HPLC and Gas Chromatography • Conducting validation testing and stability analysis • Maintaining laboratory documentation according to GLP guidelines • Using advanced analytical instruments such as ICP‑OES, ICP‑MS, and LC‑MS systems • Supporting pharmaceutical analytical method validation activities Quality Control professionals ensure that all pharmaceutical products meet defined regulatory and quality standards. Packing Department The packing department ensures pharmaceutical products are properly packaged and labeled according to regulatory and safety requirements. Key responsibilities include: • Operating pharmaceutical labeling and blister packaging machines • Managing Track & Trace systems for product identification • Conducting visual inspection of pharmaceutical vials • Supporting packaging line qualification activities • Maintaining packaging documentation records Packaging teams play a crucial role in maintaining product traceability and regulatory compliance within pharmaceutical supply chains. Eligibility / Qualifications Candidates applying for these positions must possess relevant pharmaceutical or technical educational backgrounds. Required Educational Qualifications M.Pharm, B.Pharm, B.Sc, M.Sc, Diploma in Engineering, ITI These academic programs provide candidates with foundational knowledge in pharmaceutical manufacturing processes, laboratory testing procedures, and technical equipment operations. Experience Requirements Production Department 01 – 06 Years Quality Control Department 01 – 05 Years Packing Department 0 – 05 Years Both experienced professionals and early‑career candidates are encouraged to attend the walk‑in interview. Preferred Skills Ideal candidates should demonstrate: • Knowledge of GMP and pharmaceutical manufacturing regulations • Experience working with sterile injectable manufacturing systems • Familiarity with analytical instruments such as HPLC and GC • Understanding of pharmaceutical documentation practices • Ability to work in shift‑based manufacturing environments Candidates with exposure to sterile injectable manufacturing, pharmaceutical analytical testing, or pharmaceutical packaging technologies will have an advantage. Location & Salary Job Location Emcure Pharmaceuticals Ltd. Plot No. SM‑14‑15‑16/1 GIDC Phase II Sanand, Ahmedabad Gujarat The Sanand facility is a major pharmaceutical manufacturing hub with advanced infrastructure supporting sterile injectable production. Salary Salary packages will depend on candidate qualifications, experience, and skill sets. Pharmaceutical manufacturing roles typically include competitive compensation along with career development opportunities. Application Process Interested candidates can attend the walk‑in interview directly at the company location. Walk‑In Interview Details Date: 13 March 2026 (Friday) Time: 10:00 AM – 4:00 PM Venue: Emcure Pharmaceuticals Ltd. Plot No. SM‑14‑15‑16/1 GIDC Phase II Sanand Ahmedabad, Gujarat Candidates are advised to carry: • Updated Resume • Educational certificates • Government ID proof • Experience documents (if applicable) Shortlisted candidates may proceed through technical interviews and HR evaluation rounds during the recruitment drive. Why Build a Career in Injectable Pharmaceutical Manufacturing Injectable pharmaceutical manufacturing represents one of the most technically advanced areas of the pharmaceutical industry. These facilities require strict contamination control systems, sterile manufacturing environments, and highly skilled professionals. Professionals working in injectable manufacturing gain expertise in: • Sterile pharmaceutical production technologies • Injectable formulation manufacturing processes • Pharmaceutical GMP compliance systems • Advanced pharmaceutical analytical testing • Pharmaceutical regulatory documentation These skills are highly valuable across pharmaceutical companies, contract manufacturing organizations (CMOs), and biotechnology firms worldwide. Career progression opportunities may include: • Production Supervisor • Quality Control Scientist • Pharmaceutical Validation Specialist • Pharmaceutical Operations Manager The global demand for sterile injectable medicines continues to grow rapidly, making this a promising career path for pharmaceutical professionals. Frequently Asked Questions (FAQs) Who can attend the Emcure walk‑in interview? Candidates with qualifications such as M.Pharm, B.Pharm, B.Sc, M.Sc, Diploma, or ITI with relevant pharmaceutical experience can attend the walk‑in drive. What departments are hiring? The company is hiring for Production (Injectable), Quality Control, and Packing departments. What analytical instruments are used in QC roles? QC professionals typically operate instruments such as HPLC, GC, ICP‑OES, ICP‑MS, and LC‑MS. Where is the job location? The positions are based at the Emcure Pharmaceuticals injectable manufacturing facility in Sanand, Ahmedabad. Is prior injectable manufacturing experience required? Candidates with injectable manufacturing exposure are preferred, but candidates with relevant pharmaceutical manufacturing experience may also apply. Job Summary Company Emcure Pharmaceuticals Ltd. Vacancies Production Executive, Quality Control Analyst, Packing Operator Required Education M.Pharm, B.Pharm, B.Sc, M.Sc, Diploma, ITI Experience 0 – 6 Years [...] Read more...

Virchow walk‑in Trainee Executive, Trainee Operator

March 10, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BSc BPharm ITI Fresher Jobs | Virchow Biotech Hyderabad BSc, M.Sc, BPharm, ITI fresher vacancies (50 posts) at Virchow Biotech Hyderabad for R&D, Manufacturing, QC & Engineering. Virchow Biotech Private Limited has announced a mega walk‑in recruitment drive for fresh graduates and technical diploma holders at its Skill Development Center in Hyderabad. The company is hiring Trainee Executives and Trainee Operators across multiple pharmaceutical and biotechnology departments including Biologics R&D, Injectable Manufacturing, Engineering, Quality Control, Microbiology, Packing, and Warehouse operations. This recruitment initiative targets 2023, 2024, and 2025 pass‑out candidates who want to begin their careers in the rapidly growing biopharmaceutical and injectable manufacturing industry. With approximately 50 vacancies available, the hiring drive provides a valuable entry point for candidates interested in gaining hands‑on experience in regulated pharmaceutical manufacturing environments. Virchow Biotech is recognized as one of India’s fast‑growing biotechnology companies specializing in biologics manufacturing, injectable formulations, and complex pharmaceutical development. Candidates selected through this walk‑in drive will gain exposure to GMP‑regulated pharmaceutical manufacturing systems, biologics processing technologies, sterile injectable production, and pharmaceutical quality assurance practices. For fresh graduates, roles like Trainee Executive and Trainee Operator provide the first step toward building a successful career in biopharmaceutical production, biotechnology research, pharmaceutical engineering, and regulatory compliance operations. Company Overview Virchow Biotech Pvt. Ltd. is a leading biotechnology and pharmaceutical manufacturing organization headquartered in Hyderabad, India. The company specializes in the development and production of biologic drugs, sterile injectable medicines, and complex pharmaceutical formulations used in healthcare systems worldwide. Biopharmaceutical companies such as Virchow Biotech play a crucial role in modern medicine by developing advanced therapies including recombinant proteins, vaccines, biosimilars, and injectable drug products. Manufacturing these products requires highly controlled environments, sophisticated laboratory infrastructure, and strict adherence to international regulatory standards. Virchow operates multiple state‑of‑the‑art manufacturing facilities equipped with advanced biotechnology processing equipment, sterile injectable production lines, analytical laboratories, and pharmaceutical engineering infrastructure. These facilities operate under globally recognized pharmaceutical compliance frameworks including: • Current Good Manufacturing Practices (cGMP) • Good Documentation Practices (GDP) • Pharmaceutical Quality Management Systems (QMS) • International regulatory inspection standards By maintaining strict quality and compliance standards, Virchow Biotech ensures that its pharmaceutical products meet global regulatory expectations and contribute to improving patient healthcare outcomes. The company’s focus on biologics research, injectable manufacturing technology, and pharmaceutical innovation makes it an ideal workplace for young professionals who want to develop careers in the life sciences industry. Job Role & Responsibilities Selected candidates will be placed as Trainee Executives or Trainee Operators in various technical departments within the company. The roles are designed to provide structured training and practical exposure to pharmaceutical manufacturing and biotechnology processes. Biologics Research & Development (R&D) R&D trainees support research scientists working on biological drug development and bioprocess optimization. Key responsibilities include: • Assisting scientists in biologics research projects • Supporting laboratory experiments and documentation • Maintaining laboratory equipment and testing instruments • Recording experimental data according to regulatory documentation practices • Supporting biotechnology process development activities This role provides exposure to biotechnology research techniques and biologics development processes. Injectable Manufacturing Manufacturing trainees support production activities in sterile injectable pharmaceutical manufacturing units. Key responsibilities include: • Supporting production operations for injectable drug products • Following GMP guidelines during manufacturing processes • Monitoring production equipment and manufacturing parameters • Maintaining batch manufacturing documentation • Supporting production supervisors during batch execution Injectable manufacturing environments require strict compliance with sterile production standards and pharmaceutical regulatory guidelines. Engineering Department Engineering trainees assist with maintenance and technical support activities for manufacturing equipment and plant utilities. Key responsibilities include: • Supporting plant maintenance activities • Assisting with equipment troubleshooting • Monitoring utility systems including HVAC and electrical systems • Supporting preventive maintenance schedules Engineering teams ensure that pharmaceutical production equipment operates efficiently and safely. Quality Control Laboratory Quality Control teams ensure pharmaceutical products meet quality specifications through laboratory testing and analysis. Key responsibilities include: • Assisting in laboratory testing procedures • Supporting sample preparation and documentation • Maintaining laboratory equipment • Recording analytical results and maintaining quality documentation QC professionals ensure that pharmaceutical products meet purity, potency, and regulatory quality standards. Microbiology Department Microbiology teams monitor microbial contamination within pharmaceutical manufacturing facilities. Key responsibilities include: • Supporting environmental monitoring programs • Assisting in microbiological testing procedures • Maintaining laboratory documentation and testing records Microbiology testing helps maintain sterile pharmaceutical production environments. Packing and Warehouse Operations Packing and warehouse teams ensure proper handling, storage, and distribution of pharmaceutical materials. Key responsibilities include: • Supporting packaging operations for finished pharmaceutical products • Assisting in material dispensing and inventory management • Maintaining warehouse documentation and stock records • Ensuring GMP compliance in storage and logistics operations Efficient warehouse operations support pharmaceutical supply chain management. Eligibility / Qualifications Virchow Biotech is looking for enthusiastic fresh graduates and technical professionals interested in biotechnology and pharmaceutical manufacturing careers. Required Educational Background ITI (Any Stream), Diploma Mechanical Engineering, Diploma Electrical Engineering, B.Sc Life Sciences, B.Sc Biotechnology, M.Sc Life Sciences, B.Pharm, B.Tech Mechanical Engineering, B.Tech Electrical Engineering These academic backgrounds provide the scientific and technical foundation required for pharmaceutical manufacturing and biotechnology research roles. Experience Requirement Freshers only. Candidates who graduated in 2023, 2024, or 2025 are eligible to attend the walk‑in interview. Preferred Candidate Profile Ideal candidates should demonstrate: • Basic understanding of pharmaceutical manufacturing or biotechnology processes • Willingness to work in regulated manufacturing environments • Ability to follow GMP and safety procedures • Strong teamwork and communication skills • Flexibility to work in shift‑based operations According to the company hiring notice, only male candidates are eligible for this recruitment drive. Location & Salary Job Location Virchow Biotech Pvt. Ltd. Survey No. 172 Part Gagillapur Quthbullapur Hyderabad, Telangana – 500043 The facility is located near Granules India Limited, one of the major pharmaceutical manufacturing companies in the Hyderabad industrial cluster. Salary Salary will be offered based on candidate qualification, skill set, and training performance. Entry‑level biotechnology and pharmaceutical manufacturing roles typically include structured training programs and career growth opportunities. Walk‑In Interview Details Interview Dates 13 March 2026 (Friday) 14 March 2026 (Saturday) Interview Time 9:00 AM – 11:00 AM Interview Venue Virchow Biotech Pvt. Ltd. Survey No. 172 Part Gagillapur, Quthbullapur Hyderabad – 500043 Telangana Candidates attending the walk‑in interview should carry: • Updated Resume / CV • Educational Certificates • Government ID Proof • Passport size photographs Applicants should be willing to work in shift‑based pharmaceutical manufacturing operations. Application Process Interested candidates can directly attend the walk‑in interview at the specified venue on the scheduled dates. Candidates are advised to arrive early and bring all necessary documents for verification. For candidates unable to attend the walk‑in drive, they may contact the company recruitment team for further guidance through the company’s official communication channels. Why Build a Career in Biopharmaceutical Manufacturing Biopharmaceutical manufacturing is one of the fastest growing sectors in the global healthcare industry. Companies producing biologic medicines require skilled professionals trained in biotechnology processing, pharmaceutical manufacturing, regulatory compliance, and sterile production technologies. Working in this sector allows professionals to develop expertise in areas such as: • Biologics production technology • Injectable pharmaceutical manufacturing • Biotechnology laboratory techniques • Pharmaceutical GMP compliance • Pharmaceutical process engineering Professionals trained in these fields are in high demand across pharmaceutical companies, biotechnology firms, contract research organizations, and global healthcare manufacturers. Typical career growth paths include: • Production Executive • Bioprocess Engineer • Quality Assurance Specialist • Biotechnology Research Scientist • Pharmaceutical Plant Operations Manager As biologic medicines continue to transform healthcare treatment worldwide, professionals with biopharmaceutical manufacturing expertise will remain essential to the pharmaceutical industry. Frequently Asked Questions (FAQs) Who can apply for Virchow Biotech trainee roles? Fresh graduates with ITI, Diploma, B.Sc, M.Sc, B.Pharm, or B.Tech qualifications from relevant fields can apply. What departments are hiring in this walk‑in drive? The company is hiring for R&D, Manufacturing, Engineering, Quality Control, Microbiology, Packing, and Warehouse departments. Are freshers eligible for these positions? Yes. The recruitment drive is specifically designed for fresh graduates who completed their studies in 2023, 2024, or 2025. Where is the walk‑in interview location? The interview will be conducted at Virchow Biotech Pvt. Ltd. facility located in Gagillapur, Hyderabad. What roles are offered in this recruitment drive? Candidates may be selected for Trainee Executive or Trainee Operator roles depending on qualification and department requirements. Job Summary Company Virchow Biotech Private Limited Vacancies Trainee Executive, Trainee Operator Required Education ITI, Diploma Mechanical, Diploma Electrical, B.Sc Life Sciences, M.Sc Life Sciences, B.Pharm, B.Tech Experience Freshers (2023–2025 Passouts) [...] Read more...

Fresher Walkin Drive at Bharat Serums and Vaccines

March 10, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Pune Pharma Freshers Alert: BSV Walk‑In Drive for Production Roles Pharmacy and life sciences graduates around Pune and Mumbai are watching this hiring closely. Bharat Serums and Vaccines Limited (BSV), part of the Mankind Group, has announced a walk‑in recruitment drive for Production Officers and Executives at its Ambernath manufacturing facility in Maharashtra. For B.Pharm, M.Pharm and MSc Biotechnology graduates, this hiring comes at a time when India’s biopharmaceutical manufacturing sector is expanding rapidly. Opportunities inside injectable formulations, biotech API production and plasma fractionation are becoming valuable entry points into high‑growth pharmaceutical manufacturing careers. The company is inviting candidates with 1 to 5 years of industry experience to attend the on‑site interview drive scheduled for 14th March and 15th March 2026 at the Ambernath plant in Maharashtra. Company Overview Bharat Serums and Vaccines Limited (BSV), now a part of the Mankind Pharma Group, is one of India’s established biopharmaceutical companies focused on developing specialized biological and injectable therapies. The company has built a strong presence in critical care, women’s health, fertility treatment and immunology products. Its manufacturing capabilities include plasma‑derived therapies, biotech APIs, sterile injectables and complex biologics used across global healthcare markets. Professionals joining BSV gain exposure to regulated pharmaceutical manufacturing environments, advanced biotechnology platforms and GMP‑driven production systems that support global drug supply chains. Job Role and Responsibilities Selected candidates will work in the Production Department supporting biopharmaceutical manufacturing operations at the Ambernath facility. These roles are designed for professionals involved in sterile manufacturing, upstream processing and biotech production environments. Key responsibilities include: Execute production activities related to injectable formulations and biotech APIs Operate and monitor upstream processing (USP) and downstream processing (DSP) systems Perform filtration, intermediate processing and sterile manufacturing operations Support plasma fractionation processes used in biopharmaceutical production Handle AKTA systems and related biotechnology processing equipment Assist in cell culture operations and single‑use bioreactor systems Follow GMP documentation, batch manufacturing records and regulatory compliance procedures Coordinate with quality assurance and quality control teams during production activities These responsibilities play a direct role in producing complex biologics and injectable medicines used in critical therapeutic areas. Eligibility and Educational Qualifications BSV is looking for candidates with strong academic backgrounds in pharmaceutical sciences or biotechnology disciplines. Required education includes: B.Pharm, M.Pharm, MSc Biotechnology, MSc Microbiology, Biotechnology, Microbiology, Biochemistry, Life Sciences Candidate requirements include: 1 to 5 years of experience in pharmaceutical or biotech manufacturing Hands‑on exposure to injectable formulations or biotech API production Knowledge of upstream processing (USP) or downstream processing (DSP) Experience with filtration systems, plasma fractionation or bioreactor technology preferred Familiarity with GMP documentation and pharmaceutical manufacturing compliance Strong attention to detail in sterile production environments Professionals with experience in biologics manufacturing, cell culture processing and filtration technologies will find this opportunity particularly valuable. Location and Salary The positions are based at the company’s biopharmaceutical manufacturing facility in Ambernath East, Maharashtra (421506). Walk‑In Interview Details BSV will conduct on‑site walk‑in interviews for shortlisted candidates. Interview Dates 14 March 2026 – Saturday 15 March 2026 – Sunday Interview Venue Plot No K‑27 Anand Nagar Additional MIDC Ambernath East, Maharashtra 421506 Candidates are encouraged to upload their details and CV through the official application form before attending the walk‑in drive. Application Form: https://docs.google.com/forms/d/e/1FAIpQLSeyEtxbH8N6kcOXGhKlDrNqJ-Zoi9x2G91JYQlFSlck-Xf_CQ/viewform Applicants should carry updated resumes and relevant academic documents during the interview process. Frequently Asked Questions Who can apply for the BSV Production Officer role? Candidates with B.Pharm, M.Pharm, MSc Biotechnology or MSc Microbiology qualifications and 1 to 5 years of pharmaceutical manufacturing experience can apply. Is this a walk‑in interview or online recruitment? This is an on‑site walk‑in interview drive conducted at the Ambernath manufacturing facility on 14th and 15th March 2026. What production areas are included in this role? The role covers injectable formulation manufacturing, biotech API production, plasma fractionation, upstream processing and downstream processing. Is prior biologics manufacturing experience required? Candidates with experience in biotech production, filtration systems, cell culture or bioreactor operations will have an advantage. How can candidates apply before attending the interview? Applicants can submit their details using the official application form link provided by the company before attending the walk‑in drive. Important Recruitment Disclaimer Bharat Serums and Vaccines Limited follows a strict merit‑based hiring process. The company does not charge any application fees, security deposits or payments during recruitment. Candidates receiving suspicious job offers requesting money in the name of BSV recruitment should treat them as fraudulent and avoid responding. Job Summary Company Bharat Serums and Vaccines Limited (BSV) – A Mankind Group Company Vacancies Production Officer, Production Executive Required Education B.Pharm, M.Pharm, MSc Biotechnology, MSc Microbiology, Biotechnology, Microbiology, Biochemistry, Life Sciences Experience 1–5 Years Pharmaceutical or Biotech Manufacturing Department Production – Injectable Formulations & Biotech API Interview Mode Walk‑In Interview Interview Dates 14 March 2026, 15 March 2026 Location Ambernath East, Maharashtra Application Online Form Submission + Walk‑In Interview [...] Read more...

Malladi walk-in Production, QA, QC

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BSc MSc API Jobs Walk-In | Malladi Drugs Tirupati BSc, MSc API Pharma vacancies at Malladi Drugs walk-in Hyderabad for Production, QA, QC roles with 0–8 yrs experience. Malladi Drugs & Pharmaceuticals Limited is conducting a walk-in recruitment drive for multiple technical roles across Production, Quality Assurance (QA), Quality Control (QC), and Engineering Services for its API pharmaceutical manufacturing facilities located in Tirupati and Vellore. The company is inviting candidates with life sciences and engineering backgrounds who are interested in building careers in the pharmaceutical API manufacturing industry. This walk-in hiring event is designed for both fresh graduates and experienced professionals with up to 8 years of experience in API pharmaceutical manufacturing. Selected candidates will work in regulated pharmaceutical manufacturing environments where strict Good Manufacturing Practices (GMP), process safety systems, and regulatory compliance frameworks are followed to ensure the production of high-quality pharmaceutical ingredients. API manufacturing forms the foundation of the pharmaceutical supply chain. Active Pharmaceutical Ingredients are the core chemical compounds used in finished medicines such as tablets, capsules, injections, and syrups. Professionals working in API manufacturing gain valuable expertise in chemical synthesis, pharmaceutical production operations, analytical testing, regulatory compliance, and industrial plant engineering. Candidates attending the walk-in interview will have the opportunity to join a reputed pharmaceutical company known for its strong presence in API manufacturing and global pharmaceutical supply. Company Overview Malladi Drugs & Pharmaceuticals Limited is a well-established pharmaceutical company specializing in the manufacturing of Active Pharmaceutical Ingredients (APIs) used in pharmaceutical formulations across global healthcare markets. The company has built a strong reputation for producing high-quality pharmaceutical raw materials that support the development and manufacturing of essential medicines worldwide. The organization operates advanced API manufacturing facilities equipped with modern chemical synthesis systems, quality control laboratories, and regulatory-compliant manufacturing processes. These facilities follow strict pharmaceutical regulatory frameworks including Good Manufacturing Practices (GMP), quality management systems, and global regulatory standards. Malladi Drugs supplies pharmaceutical ingredients to companies involved in the production of finished dosage forms such as tablets, capsules, injections, and oral liquids. Because APIs directly influence the quality and effectiveness of medicines, API manufacturers must maintain rigorous quality systems and highly controlled manufacturing environments. Working with Malladi Drugs provides professionals with exposure to chemical manufacturing operations, pharmaceutical process development, regulatory quality systems, and global pharmaceutical industry standards. Job Role & Responsibilities Malladi Drugs & Pharmaceuticals Limited is hiring professionals for multiple departments that support API manufacturing operations. Production – API Manufacturing Production professionals are responsible for executing chemical manufacturing processes used to produce pharmaceutical active ingredients. Key responsibilities include: • Supporting API manufacturing operations on the production floor • Monitoring chemical synthesis processes and production parameters • Maintaining batch manufacturing records and documentation • Ensuring compliance with Good Manufacturing Practices (GMP) • Handling production equipment used in chemical processing • Supporting process optimization and manufacturing efficiency Production teams ensure that pharmaceutical raw materials are manufactured consistently, safely, and efficiently. Quality Assurance (QA) Quality Assurance teams ensure that pharmaceutical manufacturing processes comply with regulatory standards and company quality systems. Key responsibilities include: • Monitoring GMP compliance across manufacturing operations • Reviewing batch manufacturing documentation • Supporting internal audits and regulatory inspections • Reviewing quality system documentation and reports • Maintaining quality management system (QMS) compliance QA professionals play a crucial role in ensuring pharmaceutical products meet strict regulatory quality standards. Quality Control (QC) Quality Control analysts perform laboratory testing to ensure pharmaceutical raw materials meet quality specifications. Key responsibilities include: • Conducting analytical testing of API samples • Performing laboratory analysis using analytical instruments • Maintaining laboratory documentation according to SOPs • Supporting stability testing and analytical method verification • Ensuring compliance with Good Laboratory Practices (GLP) QC laboratories ensure that pharmaceutical ingredients meet required purity, potency, and safety standards. Engineering Services (Electrical & Mechanical) Engineering teams support the maintenance and operation of pharmaceutical manufacturing equipment and plant utilities. Key responsibilities include: • Maintaining electrical and mechanical systems within the plant • Supporting equipment troubleshooting and maintenance • Conducting preventive maintenance activities • Ensuring continuous plant operations and reliability • Supporting utility systems used in pharmaceutical manufacturing Engineering professionals ensure reliable plant operations and minimize production downtime. Eligibility / Qualifications Malladi Drugs is looking for candidates with relevant academic backgrounds and pharmaceutical industry exposure. Required Educational Background B.Sc Chemistry, B.Sc Life Sciences, M.Sc Chemistry, M.Sc Pharmaceutical Chemistry, M.Sc Microbiology, M.Sc Biotechnology, Electrical Engineering Diploma, Mechanical Engineering Diploma, B.Tech Electrical, B.Tech Mechanical Experience Requirements Production Department Freshers to 8 Years of experience in API pharmaceutical manufacturing Quality Assurance Department 2 to 8 Years of experience in API pharmaceutical manufacturing Quality Control Department 2 to 8 Years of experience in API pharmaceutical analytical laboratories Engineering Services 2 to 8 Years of experience in pharmaceutical plant electrical or mechanical maintenance Candidates with experience working in API pharmaceutical manufacturing plants will be preferred. Required Skills Ideal candidates should demonstrate: • Knowledge of API pharmaceutical manufacturing processes • Understanding of GMP regulatory standards • Experience in chemical manufacturing operations • Familiarity with pharmaceutical documentation systems • Technical knowledge related to plant engineering systems Candidates must be capable of working in regulated pharmaceutical manufacturing environments. Location & Salary Job Location Malladi Drugs & Pharmaceuticals Limited API Manufacturing Facilities Tirupati, Andhra Pradesh Vellore, Tamil Nadu These locations host large-scale pharmaceutical manufacturing operations that support the global pharmaceutical supply chain. Salary Compensation packages depend on candidate qualifications, technical expertise, and pharmaceutical industry experience. Professionals with API manufacturing experience typically receive competitive industry salary packages. Walk-In Interview Details Interview Date 13 March 2026 (Friday) Interview Time 09:00 AM to 05:00 PM Interview Venue Hotel SVM Grand Near Bharat Petroleum Petrol Pump Plot No. 5 Part and 6 Part MSL Arcade Nizampet Road Bachupally Medchal Malkajgiri Hyderabad – 500090 Telangana Documents to Carry Candidates attending the walk-in interview should bring: • Updated resume or CV • Educational qualification certificates • Experience certificates (if applicable) • Identity proof Only candidates meeting the eligibility criteria mentioned by the company will be considered for the recruitment drive. Application Process Interested candidates can attend the walk-in interview directly at the specified location. Applicants who cannot attend the drive may contact the company HR team. Contact Person Rakesh Panja Contact Number 73585 35111 Email your CV to: careers@malladi.co.in Candidates should clearly mention their experience in API manufacturing, pharmaceutical quality systems, analytical laboratory testing, or plant engineering when submitting their application. Why Build a Career in API Pharmaceutical Manufacturing API manufacturing is one of the most important segments of the pharmaceutical industry because it provides the essential ingredients used in medicine production. Professionals working in this field gain expertise in chemical synthesis processes, pharmaceutical manufacturing systems, regulatory compliance, and industrial process engineering. API manufacturing facilities operate under strict regulatory oversight from international authorities. Professionals working in this sector develop specialized skills that are highly valuable across pharmaceutical companies and chemical manufacturing organizations worldwide. Career progression opportunities may include: • API Production Executive • Pharmaceutical Quality Assurance Manager • Analytical Quality Control Specialist • Chemical Process Development Scientist • Pharmaceutical Plant Operations Manager With the growing global demand for medicines, experienced API manufacturing professionals remain in strong demand across the pharmaceutical industry. Frequently Asked Questions (FAQs) Who can attend the Malladi Drugs walk-in interview? Candidates with BSc, MSc, engineering diplomas, or relevant qualifications and API pharmaceutical experience can attend the walk-in drive. Are freshers eligible for the production department? Yes. Fresh graduates with BSc or MSc qualifications may apply for production roles. What departments are hiring in this recruitment drive? The company is hiring for Production, Quality Assurance, Quality Control, and Engineering Services departments. Where will the selected candidates work? Selected candidates will work at Malladi Drugs API manufacturing facilities located in Tirupati and Vellore. How can candidates apply if they cannot attend the walk-in interview? Candidates can send their updated resume to the official recruitment email provided by the company. Job Summary Company Malladi Drugs & Pharmaceuticals Limited Vacancies Production Executive, QA Executive, QC Officer, Engineering Services Engineer Required Education BSc Chemistry, MSc Chemistry, MSc Microbiology, BTech Electrical, BTech Mechanical Experience Freshers to 8 Years [...] Read more...

Mehta walk‑in R&D, QA, Production

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BSc MSc API Jobs Walk‑In | Mehta API Boisar BSc, MSc API pharma vacancies at Mehta API Pvt Ltd Boisar walk‑in for R&D, QA, Production roles. Freshers to 7 yrs. Mehta API Pvt. Ltd. is conducting a walk‑in interview for multiple positions across R&D, Production, Quality Assurance, EHS, Microbiology, and Engineering functions at its API pharmaceutical manufacturing facility located in Boisar, Maharashtra. The company is inviting qualified professionals from life sciences, chemistry, and engineering backgrounds to participate in this recruitment drive. Active Pharmaceutical Ingredient (API) manufacturing plays a critical role in the global pharmaceutical supply chain. APIs are the core chemical compounds used in the formulation of finished medicines. Companies involved in API production must maintain strict Good Manufacturing Practices (GMP), regulatory compliance, and process optimization to ensure product safety and quality. This hiring drive presents an excellent opportunity for candidates ranging from fresh graduates to professionals with up to 7 years of pharmaceutical industry experience to build careers in regulated pharmaceutical manufacturing environments. Selected candidates will work in key technical areas including chemical research, manufacturing operations, environmental safety, microbiological quality monitoring, and plant maintenance. Professionals joining Mehta API will gain exposure to API process development, chemical manufacturing systems, quality compliance frameworks, and pharmaceutical production technologies used in global pharmaceutical industries. Company Overview Mehta API Pvt. Ltd. is a pharmaceutical manufacturing company specializing in the production of Active Pharmaceutical Ingredients (APIs) for domestic and international pharmaceutical markets. API manufacturing companies supply the essential raw pharmaceutical compounds that are later formulated into finished dosage forms such as tablets, capsules, injections, and syrups. The pharmaceutical industry relies heavily on high‑quality API manufacturers to ensure medicines meet strict regulatory requirements set by global authorities such as the USFDA, WHO, EMA, and other international regulatory agencies. To meet these expectations, companies invest heavily in research laboratories, modern manufacturing equipment, environmental safety systems, and robust quality assurance frameworks. Mehta API operates its manufacturing facility in Boisar, Maharashtra, one of India’s rapidly growing pharmaceutical manufacturing clusters. The facility supports research, chemical synthesis, manufacturing operations, microbiology monitoring, engineering maintenance, and regulatory quality systems that ensure pharmaceutical products are manufactured safely and efficiently. Working with Mehta API provides professionals with exposure to chemical process development, pharmaceutical manufacturing operations, regulatory compliance systems, and industrial pharmaceutical production environments. Job Role & Responsibilities Mehta API Pvt. Ltd. is recruiting professionals across several technical and operational departments within its pharmaceutical manufacturing facility. Research & Development (R&D) R&D professionals play an important role in developing and optimizing chemical synthesis processes used in API manufacturing. Key responsibilities include: • Conducting laboratory research for API process development • Supporting chemical synthesis and reaction optimization • Recording experimental observations and maintaining laboratory documentation • Supporting scale‑up activities for manufacturing processes • Ensuring laboratory activities comply with regulatory and safety guidelines R&D teams help pharmaceutical companies improve manufacturing efficiency and develop new pharmaceutical products. Analytical Research & Documentation (ARD) Analytical documentation teams ensure accurate record keeping and regulatory documentation management. Key responsibilities include: • Maintaining documentation related to analytical and research processes • Managing data entry and documentation systems • Supporting regulatory documentation preparation • Ensuring accurate documentation for laboratory and production activities Proper documentation ensures compliance with pharmaceutical regulatory guidelines and data integrity standards. Production – API Manufacturing Production professionals oversee the manufacturing processes used to produce active pharmaceutical ingredients. Key responsibilities include: • Supervising chemical manufacturing processes • Monitoring plant operations and production parameters • Maintaining batch manufacturing records • Ensuring compliance with GMP manufacturing standards • Supporting process optimization and production efficiency Production supervisors and executives play a key role in ensuring pharmaceutical compounds are manufactured consistently and safely. Quality Assurance (QA) Quality assurance professionals ensure that manufacturing processes comply with pharmaceutical regulatory guidelines and internal quality standards. Key responsibilities include: • Reviewing batch manufacturing documentation • Monitoring GMP compliance across manufacturing operations • Supporting internal audits and regulatory inspections • Reviewing quality documentation and reports • Maintaining pharmaceutical quality management systems QA professionals ensure that pharmaceutical products meet required quality standards before they move to the next stage of production or distribution. Microbiology Microbiology professionals monitor microbial contamination and environmental conditions within pharmaceutical manufacturing facilities. Key responsibilities include: • Performing microbiological testing of environmental samples • Monitoring microbial contamination within production areas • Supporting environmental monitoring programs • Maintaining microbiology laboratory documentation Microbiological monitoring is critical to maintaining sterile and contamination‑free pharmaceutical manufacturing environments. Environmental Health & Safety (EHS) EHS professionals ensure that pharmaceutical manufacturing plants operate safely and comply with environmental regulations. Key responsibilities include: • Monitoring workplace safety conditions • Implementing environmental safety policies • Conducting safety training programs • Maintaining compliance with industrial safety regulations • Supporting risk assessment and safety audits These responsibilities ensure safe operations within chemical and pharmaceutical manufacturing plants. Engineering & Technical Maintenance Engineering professionals maintain plant infrastructure and ensure continuous operations of manufacturing equipment. Key responsibilities include: • Maintaining HVAC systems and plant electrical systems • Troubleshooting equipment failures • Performing preventive maintenance • Ensuring reliable plant utility operations Technical maintenance teams play a vital role in maintaining efficient pharmaceutical manufacturing operations. Eligibility / Qualifications Mehta API Pvt. Ltd. is seeking candidates with relevant academic backgrounds and pharmaceutical or industrial experience. Required Educational Background MSc Chemistry, BSc Chemistry, BSc Life Sciences, MSc Microbiology, BCom, BA, ITI Electrical, ITI Mechanical, Diploma Engineering, ADIS Industrial Safety Candidates with pharmaceutical API manufacturing exposure will be preferred. Experience Requirements R&D Officer Freshers to 3 Years R&D Executive 5 to 7 Years Production Supervisor 3 to 4 Years Production Executive 6 to 7 Years QA Senior Officer 4 to 5 Years EHS Officer 2 to 3 Years HVAC Technician 2 to 3 Years Electrician 3 to 4 Years Microbiology Officer Freshers Production Operator 4 to 5 Years Required Skills Ideal candidates should demonstrate: • Knowledge of API manufacturing processes • Understanding of GMP pharmaceutical standards • Experience in chemical production operations • Familiarity with pharmaceutical documentation systems • Ability to work within regulated manufacturing environments Candidates from pharmaceutical API industry backgrounds are strongly preferred. Location & Salary Job Location Mehta API Pvt. Ltd. Gut No. 571, 546, 519 & 520 Village Kumbhavali MIDC Boisar Dist. Palghar Maharashtra – 401506 Boisar is an important pharmaceutical and chemical manufacturing hub that hosts multiple API and formulation manufacturing companies. Salary Compensation packages depend on candidate experience, technical expertise, and role responsibilities. Professionals with pharmaceutical API manufacturing experience often receive competitive industry salary packages. Walk‑In Interview Details Interview Date 13 March 2026 (Friday) Interview Timing 11:00 AM to 4:00 PM Interview Venue Mehta API Pvt. Ltd. Gut No. 571, 546, 519 & 520 Village Kumbhavali MIDC Boisar Palghar District Maharashtra – 401506 Documents to Carry Candidates attending the interview should bring: • Updated resume or CV • Educational qualification certificates • Experience certificates (if applicable) • Identity proof Only male candidates are required for the current hiring drive according to company hiring requirements. Application Process Interested candidates can attend the walk‑in interview directly at the specified venue. Applicants who want to inquire about the recruitment process may contact the HR team. Contact Number: 8956468343 Candidates should ensure their resume clearly highlights experience in API manufacturing, pharmaceutical research, production supervision, quality assurance, or microbiology testing. Why Build a Career in API Manufacturing Active Pharmaceutical Ingredient manufacturing is one of the most critical sectors of the pharmaceutical industry. API manufacturers supply the essential chemical components used to produce medicines across global healthcare systems. Professionals working in API manufacturing gain valuable experience in chemical synthesis, process optimization, pharmaceutical quality compliance, industrial safety systems, and regulatory documentation. Typical career progression may include: • API Production Executive • Pharmaceutical Process Development Scientist • Quality Assurance Compliance Manager • Chemical Manufacturing Specialist • Pharmaceutical Plant Operations Manager With growing global demand for medicines, professionals trained in API manufacturing remain highly valuable across pharmaceutical companies and chemical manufacturing industries. Frequently Asked Questions (FAQs) Who can attend the Mehta API walk‑in interview? Candidates with BSc, MSc, ITI, Diploma, or relevant technical qualifications and pharmaceutical manufacturing experience can attend. Are freshers eligible for any roles? Yes. Fresh graduates may apply for R&D Officer and Microbiology Officer roles. What departments are hiring in this recruitment drive? The company is hiring for R&D, Production, Quality Assurance, Microbiology, EHS, Engineering, and Documentation roles. Where is the interview location? The walk‑in interview will be conducted at the Mehta API manufacturing facility located in Boisar, Maharashtra. What industry experience is preferred? Candidates with pharmaceutical API manufacturing experience are preferred. Job Summary Company Mehta API Pvt. Ltd. Vacancies R&D Officer, R&D Executive, EHS Officer, ARD Officer, Production Supervisor, Production Executive, QA Sr Officer, Micro Officer, HVAC Technician, Electrician, Production Operator Required Education MSc Chemistry, BSc Chemistry, MSc Microbiology, BCom, BA, ITI, Diploma, ADIS Experience Freshers to 7 Years [...] Read more...

Aspiro walk‑in Injectable Production & Warehouse

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BSc BPharm Injectable Production Jobs | Aspiro Pharma BSc, ITI, Diploma, BPharm vacancies in Injectable Production & Warehouse at Aspiro Pharma walk‑in Hyderabad, 2–12 yrs exp. Aspiro Pharma Limited is conducting a walk‑in recruitment drive for multiple roles in Injectable Production and Warehouse Operations at its USFDA‑approved pharmaceutical manufacturing facility located in Siddipet District, Telangana. The company is inviting qualified professionals with backgrounds in pharmaceutical sciences, life sciences, and engineering support functions to join its growing injectable manufacturing team. This hiring drive presents an excellent opportunity for candidates with 2 to 12 years of experience in sterile injectable manufacturing to work in a globally regulated pharmaceutical environment. Aspiro Pharma operates a modern sterile injectable facility that complies with international regulatory standards such as USFDA, GMP, and global pharmaceutical quality regulations. Professionals selected through this walk‑in drive will work with advanced manufacturing systems used for vial filling, lyophilization, sterile filtration, compounding, and packaging of injectable medicines. Sterile injectable manufacturing is one of the most technically demanding areas of the pharmaceutical industry. It requires strict environmental control, advanced equipment, validated processes, and highly trained personnel to ensure patient safety. Working in injectable manufacturing exposes professionals to high‑value pharmaceutical production systems, regulatory compliance frameworks, and quality‑driven operations used in global pharmaceutical markets. Candidates with experience in sterile production processes such as filtration, filling, stoppering, vial washing, autoclave operations, lyophilization, and compounding will find this opportunity particularly beneficial for long‑term career growth in pharmaceutical manufacturing. Company Overview Aspiro Pharma Limited is a globally recognized pharmaceutical manufacturing company specializing in sterile injectable formulations. The company operates USFDA‑approved manufacturing facilities and supplies high‑quality injectable medicines to regulated international markets. The organization focuses on producing complex sterile pharmaceutical products including lyophilized injections, liquid injectables, ophthalmic products, and suspension formulations. These products are used in hospitals and healthcare institutions worldwide, making quality and regulatory compliance critical aspects of the manufacturing process. Aspiro Pharma’s injectable manufacturing facilities are designed according to international regulatory standards and incorporate advanced production technologies such as automated filling lines, sterile filtration systems, lyophilizers, and aseptic processing equipment. The company is also recognized as a Great Place to Work Certified organization, reflecting its focus on employee development, workplace culture, and professional growth opportunities. Professionals joining Aspiro Pharma gain valuable exposure to sterile pharmaceutical manufacturing, GMP compliance systems, regulatory audits, and advanced injectable production technologies. Job Role & Responsibilities Aspiro Pharma is hiring across two critical departments within its injectable manufacturing operations: Production and Warehouse. Production – Sterile Injectable Manufacturing Production professionals are responsible for executing sterile manufacturing operations on the shop floor. These roles ensure that injectable products are manufactured safely, efficiently, and in compliance with pharmaceutical regulatory standards. Key responsibilities include: • Operating sterile manufacturing equipment used for injectable formulations • Supporting shop floor operations including filtration, filling, sealing, and stoppering • Handling equipment used for vial washing and autoclave sterilization • Supporting lyophilization (freeze drying) processes for injectable products • Performing compounding and solution preparation activities • Monitoring production parameters and batch manufacturing processes • Ensuring compliance with Good Manufacturing Practices (GMP) • Maintaining batch manufacturing documentation and production records Production operators and supervisors work closely with quality assurance teams to maintain aseptic manufacturing standards. Production Supervision & Operations Management Senior production professionals oversee sterile manufacturing processes and ensure that production operations run smoothly. Key responsibilities include: • Supervising sterile production shop floor activities • Monitoring production schedules and manufacturing efficiency • Providing training and guidance to production operators • Ensuring compliance with quality management systems (QMS) • Coordinating with quality assurance and engineering teams • Supporting process improvements and operational efficiency Supervisory roles also involve ensuring strict adherence to aseptic manufacturing guidelines and sterile environment protocols. Warehouse Operations – Injectable Manufacturing Warehouse professionals manage raw materials, packaging materials, and finished goods within the pharmaceutical manufacturing facility. Key responsibilities include: • Handling Raw Materials (RM) and Packaging Materials (PM) • Dispensing raw materials and packaging materials for production • Managing warehouse inventory systems • Handling consumables and engineering materials • Maintaining documentation for warehouse operations • Supporting finished goods dispatch and storage • Managing warehouse quality systems and compliance • Working with SAP inventory management systems Warehouse professionals play a crucial role in maintaining traceability, inventory control, and material availability for pharmaceutical production. Eligibility / Qualifications Aspiro Pharma is looking for candidates with relevant educational backgrounds and experience in pharmaceutical manufacturing environments. Required Educational Background B.Sc Life Sciences, B.Sc Chemistry, B.Pharm, M.Pharm, D.Pharm, ITI Engineering, Diploma Engineering, MBA Operations, B.Com Candidates with experience in sterile injectable manufacturing will be preferred. Experience Requirements Production Operators / Sr Operators 2 to 7 Years of experience in injectable production operations Production Supervisors (Sr Officer – Assistant Manager) 2 to 12 Years of experience in sterile injectable manufacturing supervision Warehouse Officers / Executives 3 to 10 Years of experience in pharmaceutical warehouse operations Required Skills The ideal candidate should demonstrate: • Knowledge of sterile injectable manufacturing processes • Experience with vial filling, lyophilization, and filtration systems • Understanding of GMP and pharmaceutical compliance requirements • Experience with pharmaceutical warehouse inventory systems • Familiarity with SAP for material management • Ability to work in regulated pharmaceutical environments Candidates should also be willing to work in shift‑based manufacturing operations. Location & Salary Job Location Aspiro Pharma Limited Injectable Manufacturing Facility Karkapatla Village Markook Mandal Siddipet District Telangana, India This facility supports large‑scale sterile injectable manufacturing for global pharmaceutical markets. Interview Location BE Skill Development Center Rail Nagar Airforce Road Bolarum Secunderabad Hyderabad – 500010 Salary Salary packages depend on candidate experience, technical expertise, and exposure to sterile pharmaceutical manufacturing operations. Professionals working in injectable manufacturing environments often receive competitive compensation packages due to the specialized nature of sterile production systems. Walk‑In Interview Details Interview Date 15 March 2026 (Sunday) Interview Time 09:00 AM to 04:00 PM Candidates attending the interview should bring: • Updated resume • Educational qualification certificates • Experience documents • Identity proof Applicants who are unable to attend the walk‑in drive may send their updated CV through email. Application Process Interested candidates who cannot attend the interview can share their resumes through email. Send your CV to: Hemasundar.i@hetero.com Candidates should clearly mention their experience in sterile injectable production, pharmaceutical warehouse operations, or aseptic manufacturing environments while submitting their resume. Why Build a Career in Sterile Injectable Manufacturing Sterile injectable manufacturing is one of the most specialized sectors within the pharmaceutical industry. Injectable medicines require extremely strict manufacturing conditions to ensure sterility and patient safety. Professionals working in this field gain expertise in aseptic manufacturing, sterile processing, regulatory compliance, and advanced pharmaceutical production technologies. Career progression opportunities in injectable manufacturing may include: • Production Executive – Sterile Manufacturing • Injectable Manufacturing Specialist • Quality Assurance Professional – Sterile Operations • Pharmaceutical Operations Manager • Sterile Manufacturing Plant Manager As global demand for injectable medicines continues to grow, professionals with experience in sterile pharmaceutical manufacturing remain highly valuable across pharmaceutical companies worldwide. Frequently Asked Questions (FAQs) Who can attend the Aspiro Pharma walk‑in drive? Candidates with BSc, BPharm, MPharm, DPharm, ITI, or Diploma qualifications and relevant injectable manufacturing experience can attend. What departments are hiring in this recruitment drive? Aspiro Pharma is hiring for Production (Injectable Manufacturing) and Warehouse departments. What experience is required for production roles? Candidates should have experience working with sterile injectable manufacturing operations such as filtration, filling, sealing, and lyophilization. Is warehouse experience required for warehouse roles? Yes. Candidates should have experience handling raw materials, packaging materials, and SAP‑based warehouse management systems. How can candidates apply if they cannot attend the walk‑in interview? Candidates can send their updated resume to the official recruitment email provided by the company. Job Summary Company Aspiro Pharma Limited Vacancies Production Operator, Sr Operator, Production Officer, Assistant Manager Production, Warehouse Officer, Warehouse Executive Required Education BSc Life Sciences, BSc Chemistry, BPharm, MPharm, DPharm, ITI, Diploma, MBA, BCom Experience 2–12 Years [...] Read more...

Honour walk‑in API production & EHS

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BSc MSc BTech API Jobs Walk‑In | Honour Lab Pune BSc, MSc Chemistry, BTech Chemical API production & EHS vacancies at Honour Lab walk‑in Hyderabad for Pune units. 8–14 yrs experience. Honour Lab Ltd. is conducting a walk‑in recruitment drive for experienced pharmaceutical professionals to support its Active Pharmaceutical Ingredient (API) manufacturing units in Pune. The company is hiring across multiple technical departments including Production, Environment Health & Safety (EHS), Electrical Engineering, and Technical Services Department (TSD). This hiring event provides an opportunity for professionals with strong experience in pharmaceutical API manufacturing, plant engineering, process optimization, and regulatory compliance to join a fast‑growing pharmaceutical manufacturing organization. Candidates with chemistry, chemical engineering, or electrical engineering backgrounds who have worked in regulated pharmaceutical production environments are encouraged to attend. API manufacturing facilities are among the most complex operations in the pharmaceutical industry. They require strict adherence to GMP standards, robust safety systems, process optimization expertise, and highly trained technical professionals to maintain safe and efficient manufacturing processes. By joining Honour Lab Ltd., candidates gain exposure to advanced API manufacturing technology, global regulatory compliance systems, and large‑scale pharmaceutical production operations. Company Overview Honour Lab Ltd. is a rapidly growing pharmaceutical company specializing in the manufacturing of Active Pharmaceutical Ingredients (APIs) for global healthcare markets. The organization supplies pharmaceutical intermediates and APIs to regulated markets and collaborates with pharmaceutical companies across the world to support drug development and manufacturing supply chains. The company operates multiple manufacturing facilities equipped with advanced chemical synthesis technology and modern pharmaceutical production systems. These facilities follow strict regulatory frameworks including Good Manufacturing Practices (GMP), environmental safety standards, and international pharmaceutical compliance guidelines. Honour Lab focuses strongly on innovation, process efficiency, and safe manufacturing practices within the pharmaceutical chemical industry. By investing in advanced chemical engineering capabilities and strong environmental safety programs, the organization ensures that pharmaceutical ingredients are manufactured responsibly and efficiently. The company also promotes inclusive workplace policies and does not support discrimination in recruitment or employment practices, ensuring equal opportunities for professionals regardless of background or identity. Job Role & Responsibilities Honour Lab Ltd. is recruiting experienced professionals across multiple departments supporting API manufacturing operations. Environment Health & Safety (EHS) EHS professionals ensure that pharmaceutical manufacturing plants operate safely and comply with environmental regulations and safety standards. Key responsibilities include: • Conducting safety risk assessments such as HAZOP, ABRA, and HIRA • Monitoring safety performance indicators and compliance metrics • Implementing environmental health and safety policies • Conducting safety training programs for plant employees • Organizing mock drills and emergency response exercises • Maintaining safety documentation within Integrated Management Systems (IMS) • Ensuring compliance with GMP and regulatory safety requirements These activities ensure that pharmaceutical manufacturing plants operate safely while protecting workers, communities, and the environment. Production – API Manufacturing Production professionals are responsible for executing chemical synthesis processes used in pharmaceutical API manufacturing. Key responsibilities include: • Managing chemical production operations in API manufacturing plants • Supervising process operations and batch manufacturing activities • Monitoring production parameters and process efficiency • Ensuring compliance with GMP and manufacturing documentation • Supporting process troubleshooting and production optimization Professionals in this role ensure that pharmaceutical active ingredients are manufactured efficiently and safely according to strict quality standards. Electrical Engineering Electrical engineering teams maintain plant electrical systems and ensure uninterrupted operations in pharmaceutical manufacturing facilities. Key responsibilities include: • Troubleshooting electrical equipment used in API plants • Maintaining electrical systems for production equipment • Supporting plant maintenance and reliability engineering • Conducting preventive maintenance activities • Ensuring electrical system safety and compliance Electrical engineers play a critical role in maintaining reliable plant operations and minimizing production downtime. Technical Services Department (TSD) Technical Services teams focus on improving manufacturing efficiency, optimizing processes, and supporting scale‑up activities. Key responsibilities include: • Supporting process scale‑up activities • Optimizing chemical manufacturing processes • Identifying opportunities for cost reduction in production • Improving plant productivity and operational efficiency • Supporting technical transfer and process improvement initiatives TSD professionals contribute directly to innovation and operational excellence within pharmaceutical manufacturing environments. Eligibility / Qualifications Honour Lab Ltd. is seeking experienced professionals with relevant educational backgrounds and pharmaceutical industry exposure. Required Educational Background BSc Chemistry, MSc Chemistry, BTech Chemical Engineering, BTech Electrical Engineering, Diploma Electrical Engineering, ITI Electrical, ADIS (Advanced Diploma in Industrial Safety) Experience Requirements EHS Department 8–12 Years of experience in pharmaceutical or chemical manufacturing safety systems Production Department 8–14 Years of experience in pharmaceutical API manufacturing operations Electrical Engineering 8–10 Years of experience in pharmaceutical plant maintenance and electrical systems Technical Services Department (TSD) 10–14 Years of experience in chemical process optimization and scale‑up activities Required Skills Ideal candidates should demonstrate: • Strong understanding of pharmaceutical API manufacturing operations • Knowledge of chemical process optimization and scale‑up • Experience with plant safety systems and risk assessments • Understanding of GMP documentation and regulatory compliance • Expertise in troubleshooting manufacturing or engineering systems Candidates must have prior experience in pharmaceutical API manufacturing environments. Location & Salary Job Location Honour Lab Ltd. Pune API Units India Interview Location 8‑3‑166/7/5 Vikaspuri Erragadda Hyderabad – 500038 Telangana, India The Pune manufacturing units support large‑scale API production while the Hyderabad location hosts the walk‑in recruitment event. Salary Salary packages depend on candidate experience, technical expertise, and industry exposure. Professionals with strong API manufacturing experience and engineering expertise typically receive competitive compensation packages within the pharmaceutical industry. Walk‑In Interview Details Interview Dates 14 March 2026 (Saturday) 15 March 2026 (Sunday) Interview Timing 09:30 AM to 04:00 PM Candidates attending the walk‑in interview should bring: • Updated resume • Educational qualification certificates • Experience certificates • Identity proof Applicants should highlight their experience in API manufacturing, process safety systems, or plant engineering within their resume. Application Process Interested candidates can attend the walk‑in interview directly at the specified location. Candidates may also send their resumes through email for HR review. Email your CV to: hr.3b@honourlab.com Contact Numbers 9154113739 9030267272 Company Website honourlab.com Why Build a Career in API Manufacturing Active Pharmaceutical Ingredient manufacturing is one of the most critical sectors of the pharmaceutical industry. API manufacturers supply the essential chemical compounds that are later formulated into finished medicines used worldwide. Professionals working in API manufacturing gain expertise in chemical synthesis processes, plant safety systems, pharmaceutical regulatory compliance, and process engineering. These skills are highly valuable across pharmaceutical companies, contract manufacturing organizations, and global chemical manufacturing industries. Typical career progression includes: • Production Manager – API Manufacturing • Process Development Specialist • Plant Engineering Manager • Environmental Health & Safety Leader • Pharmaceutical Technical Services Manager With global demand for pharmaceutical ingredients continuing to grow, skilled professionals in API manufacturing remain highly valuable within the pharmaceutical and chemical industries. Frequently Asked Questions (FAQs) Who can attend the Honour Lab walk‑in interview? Candidates with BSc, MSc Chemistry, BTech Chemical Engineering, or Electrical Engineering qualifications and relevant experience in API manufacturing can attend. What departments are hiring in this recruitment drive? The company is hiring for EHS, Production, Electrical Engineering, and Technical Services Department roles. Where will the selected candidates work? Selected candidates will work at Honour Lab’s API manufacturing units located in Pune. What experience is required for these roles? Depending on the department, candidates must have between 8 and 14 years of pharmaceutical or chemical manufacturing experience. How can candidates apply if they cannot attend the interview? Candidates can send their updated resumes to the official HR email address provided by the company. Job Summary Company Honour Lab Ltd. Vacancies EHS Executive, Production Executive, Electrical Engineering Executive, Technical Services Manager Required Education BSc Chemistry, MSc Chemistry, BTech Chemical Engineering, BTech Electrical Engineering, Diploma Electrical, ITI Electrical Experience 8–14 Years depending on role [...] Read more...

Granules walk‑in Production, QC, Engineering

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BSc BPharm ITI OSD Walk‑In Vacancies | Granules Hyderabad BSc, BPharm, ITI, Diploma candidates – multiple Production, QC, Engineering vacancies at Granules India walk‑in Hyderabad. Granules India Limited is conducting a walk‑in interview for multiple positions across Production, Warehouse, Engineering, an d Quality Control departments at its OSD (Oral Solid Dosage) formulation manufacturing facility in Hyderabad. The company is inviting candidates with qualifications such as ITI, Diploma, D.Pharm, B.Sc, B.Pharm, and M.Sc who have experience working in pharmaceutical formulation manufacturing environments. This hiring initiative aims to strengthen manufacturing operations at Granules India’s Gagillapur unit, a facility known for its large‑scale pharmaceutical production systems and regulatory compliant manufacturing infrastructure. Professionals selected through this recruitment drive will work with advanced pharmaceutical equipment used in tablet compression, granulation, coating, capsule filling, packaging, and analytical laboratory testing. The walk‑in interview provides an excellent opportunity for candidates with 2–5 years of pharmaceutical formulation experience to build careers in globally regulated pharmaceutical manufacturing environments. Candidates currently working in technical contract services with formulation production exposure are also encouraged to attend the interview. Company Overview Granules India Limited is a globally recognized pharmaceutical manufacturing company specializing in large‑scale production of Active Pharmaceutical Ingredients (APIs), Pharmaceutical Formulation Intermediates (PFIs), and Finished Dosage Formulations (FDFs). The company has established itself as one of the major pharmaceutical exporters from India, supplying high‑quality medicines to global markets. With multiple USFDA‑approved manufacturing facilities, Granules India maintains strict regulatory compliance standards required by international pharmaceutical authorities including USFDA, EMA, and WHO‑GMP. The company supplies pharmaceutical products to healthcare markets across North America, Europe, and several other regions worldwide. Granules India focuses heavily on operational efficiency, large‑scale pharmaceutical production technology, and quality‑driven manufacturing systems. The Gagillapur manufacturing facility in Hyderabad is equipped with advanced production lines for oral solid dosage formulations including tablets and capsules. Working at Granules India provides pharmaceutical professionals with exposure to modern manufacturing technologies, automated production systems, regulatory compliant quality control laboratories, and international pharmaceutical regulatory standards. Job Role & Responsibilities Granules India is hiring candidates across several key pharmaceutical departments including Production, Warehouse, Engineering, and Quality Control. Production – OSD Formulations Production operators are responsible for executing pharmaceutical manufacturing processes for tablets and capsules using specialized production equipment. Key responsibilities include: • Operating granulation equipment including RMG, FBP, and FBD systems • Performing Wurster coating and roll compactor operations • Handling tablet compression machines • Operating coating equipment for tablet formulations • Ensuring compliance with GMP manufacturing standards • Maintaining batch manufacturing records and production documentation Candidates may work on machines such as: • Hata • Fette • Korsch • Sejong • Killian • Cadmach These machines are widely used in tablet compression and pharmaceutical manufacturing lines. Packaging Operations Packaging operators ensure pharmaceutical products are packed safely and efficiently according to regulatory packaging standards. Key responsibilities include: • Operating blister packaging and bottle packing lines • Handling automated packaging machines • Monitoring packaging quality and compliance • Maintaining packaging batch documentation • Ensuring proper labeling and product traceability Packaging machines used may include: • Uhlmann • IMA • BQS • Pharmapack • Countec • CVC Capsule Filling & Inspection Operators in capsule production handle capsule filling systems and inspection processes. Key responsibilities include: • Operating capsule filling machines • Monitoring capsule inspection and check‑weighing systems • Ensuring capsule sealing and printing quality • Maintaining production documentation Equipment used may include: • AF90T • AF150T • ZRO 200 • TTS systems • ACG capsule check‑weighers Warehouse Operations Warehouse professionals manage pharmaceutical raw materials, packaging materials, and finished goods inventory. Key responsibilities include: • Handling RM (Raw Material), PM (Packaging Material), and FG (Finished Goods) • Maintaining warehouse inventory records • Ensuring proper storage conditions for pharmaceutical materials • Supporting material dispatch and documentation processes Engineering Department Engineering teams support maintenance and operation of pharmaceutical manufacturing utilities and production equipment. Key responsibilities include: • Maintaining pharmaceutical production equipment • Supporting utility systems and water systems • Conducting preventive maintenance activities • Troubleshooting equipment breakdowns • Supporting process maintenance operations Quality Control (QC) Quality Control analysts perform analytical testing to ensure pharmaceutical products meet required quality standards. Key responsibilities include: • Performing analytical testing using instruments such as HPLC and GC • Supporting LCMS and GCMS analytical methods • Conducting laboratory sample testing • Maintaining analytical laboratory documentation • Ensuring compliance with Good Laboratory Practices (GLP) Eligibility / Qualifications Granules India is seeking candidates with relevant pharmaceutical qualifications and formulation manufacturing experience. Required Educational Background ITI, Diploma in Engineering, D.Pharm, B.Sc Chemistry, B.Sc Life Sciences, B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Microbiology Experience Requirements Production / Packaging / Capsule Filling 2–5 Years of experience in OSD formulation manufacturing Warehouse 2–5 Years in pharmaceutical material handling operations Engineering 2–5 Years in pharmaceutical process maintenance and utility systems Quality Control 2–5 Years in pharmaceutical analytical laboratory operations Candidates must have experience working in oral solid dosage (OSD) pharmaceutical facilities. Required Skills Ideal candidates should demonstrate: • Knowledge of OSD formulation manufacturing processes • Experience with pharmaceutical production machinery • Understanding of GMP regulatory standards • Analytical instrument handling skills for QC roles • Willingness to work in rotational shift operations Candidates currently working in technical contract services with formulation production experience are also eligible to attend the interview. Location & Salary Job Location Granules India Limited Gagillapur Unit Dundigal Hyderabad – 500043 Telangana, India Hyderabad is one of the largest pharmaceutical manufacturing hubs in India and hosts several global pharmaceutical companies and biotechnology organizations. Salary Compensation packages for these roles depend on candidate experience, machine expertise, and pharmaceutical industry exposure. Employees working in regulated pharmaceutical facilities typically receive competitive salaries along with growth opportunities in production operations and quality systems. Walk‑In Interview Details Interview Date 14 March 2026 (Saturday) Interview Time 10:00 AM to 1:00 PM Interview Venue Granules India Ltd Gagillapur Unit Dundigal Hyderabad – 500043 Phone 08418 696400 Documents to Carry Candidates attending the interview must bring photocopies of: • Updated resume • Latest increment letter • Last three months salary slips • Previous organization relieving letters and experience certificates • Educational qualification certificates • Aadhaar Card and PAN Card Candidates must be willing to work in shift operations. Spot offers may be provided to selected candidates, subject to document verification. Application Process Candidates interested in the opportunity can attend the walk‑in interview directly at the given location. Those who cannot attend may contact the company through official HR channels mentioned during the interview announcement. Applicants should ensure their resume clearly highlights experience in pharmaceutical formulation production, machine operation, analytical testing, or warehouse management within OSD manufacturing facilities. Why Build a Career with Granules India Working with Granules India allows pharmaceutical professionals to gain exposure to global pharmaceutical manufacturing standards, large‑scale production technology, and regulated quality control environments. The company’s strong presence in international pharmaceutical markets provides employees with valuable experience in regulatory compliance systems and pharmaceutical production technologies. Professionals trained in OSD manufacturing environments often progress into roles such as: • Production Executive • Pharmaceutical Manufacturing Specialist • Quality Control Analyst • Process Maintenance Engineer • Warehouse Operations Manager With continuous growth in the pharmaceutical industry, skilled professionals with experience in GMP‑compliant manufacturing systems remain highly valuable in global healthcare markets. Frequently Asked Questions (FAQs) Who can attend the Granules India walk‑in interview? Candidates with ITI, Diploma, DPharm, BSc, BPharm, MSc, or MPharm qualifications and OSD formulation experience can attend. What departments are hiring in this recruitment drive? The company is hiring for Production, Packaging, Warehouse, Engineering, and Quality Control departments. Is OSD formulation experience mandatory? Yes. Only candidates with oral solid dosage manufacturing experience will be considered. What analytical instruments should QC candidates know? Candidates should have experience with analytical instruments such as HPLC, GC, LCMS, and GCMS. What documents should candidates bring for the interview? Applicants must bring resumes, salary slips, experience certificates, educational documents, and identity proofs. Job Summary Company Granules India Limited Vacancies Production Operator, Packaging Operator, Capsule Filling Operator, Warehouse Officer, Engineering Executive, Quality Control Officer Required Education ITI, Diploma, DPharm, BSc Chemistry, BPharm, MSc Chemistry, MPharm Experience 2–5 Years [...] Read more...

BioMatrix Walk‑In QC QA

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now MSc BPharm QC QA Walk‑In Vacancies | BioMatrix Ahmedabad MSc, BPharm, MPharm QC & QA vacancies at BioMatrix Healthcare walk‑in interview in Ahmedabad. Experience 0–10 years. BioMatrix Healthcare Pvt. Ltd. is conducting a walk‑in interview to hire professionals for its Quality Control (QC) and Quality Assurance (QA) departments at its pharmaceutical manufacturing facility in Ahmedabad, Gujarat. The company is inviting candidates with relevant pharmaceutical qualifications such as M.Sc, B.Pharm, and M.Pharm to join its regulated manufacturing operations that support global pharmaceutical markets. BioMatrix Healthcare is a 100% export‑oriented pharmaceutical company engaged in research, development, and manufacturing of oral solid dosage forms, liquid formulations, and dry syrups. With multiple international regulatory approvals including WHO‑GMP, EU‑GMP, Health Canada, ANVISA, UK‑MHRA, and USFDA compliance, the company has established a strong global presence across Europe, Africa, and CIS regions. The walk‑in interview offers excellent career opportunities for fresh graduates as well as experienced pharmaceutical professionals who want to work in quality control laboratories or quality assurance operations within globally regulated pharmaceutical manufacturing facilities. Company Overview BioMatrix Healthcare Private Limited is a globally recognized pharmaceutical manufacturing company headquartered in Ahmedabad, Gujarat, India. Established in 2007 with the vision of “Supporting Life Worldwide,” the company focuses on developing high‑quality pharmaceutical formulations for global healthcare markets. The organization operates advanced pharmaceutical manufacturing facilities equipped with modern production technology and regulatory‑compliant quality systems. BioMatrix manufactures a wide range of oral solid dosage forms, liquid formulations, and dry syrups that are exported to more than 30 countries worldwide. The company has successfully achieved more than 1000 product registrations and currently maintains over 450 pharmaceutical products under registration across global markets. With regulatory accreditations from WHO‑GMP, EU‑GMP, Health Canada, and compliance with global regulatory bodies such as USFDA, ANVISA, and UKMHRA, BioMatrix continues to expand its presence in regulated international markets. Working at BioMatrix Healthcare provides pharmaceutical professionals with exposure to international regulatory standards, advanced pharmaceutical manufacturing systems, and quality management frameworks that ensure global compliance. Job Role & Responsibilities BioMatrix Healthcare is hiring professionals for two major pharmaceutical departments: Quality Control (QC) and Quality Assurance (QA). Quality Control (QC) Quality Control analysts are responsible for analytical testing of pharmaceutical products to ensure they meet strict quality standards before release. Key responsibilities include: • Operating analytical instruments such as High Performance Liquid Chromatography (HPLC) • Performing pharmaceutical analytical testing of samples • Handling analytical laboratory instruments independently • Ensuring compliance with Good Laboratory Practices (GLP) • Preparing laboratory documentation according to SOPs and protocols • Maintaining analytical data records and regulatory documentation These activities ensure pharmaceutical products meet required purity, potency, and stability standards. Quality Assurance (QA) Quality Assurance professionals ensure that pharmaceutical manufacturing processes follow strict regulatory compliance guidelines. Key responsibilities include: • Performing in‑process quality assurance (IPQA) activities • Monitoring OSD manufacturing operations including granulation, compression, and coating • Performing line clearance before batch initiation and after batch completion • Verifying cleanliness of equipment and manufacturing areas • Ensuring manufacturing operations comply with GMP requirements • Maintaining QA documentation according to regulatory guidelines These responsibilities ensure that pharmaceutical products are manufactured according to approved quality standards. Eligibility / Qualifications BioMatrix Healthcare is looking for dedicated candidates with academic backgrounds in pharmaceutical sciences and analytical chemistry. Required Educational Background MSc Chemistry, MSc Analytical Chemistry, MSc Pharmaceutical Chemistry, BPharm, MPharm, MSc Life Sciences Candidates with strong knowledge of pharmaceutical manufacturing processes, analytical chemistry techniques, and regulatory documentation practices will be preferred. Experience Requirements Quality Control Department 0 to 10 Years Quality Assurance Department 2 to 10 Years Fresh graduates may apply for trainee positions while experienced professionals may be considered for officer or executive roles. Required Skills The ideal candidate should demonstrate: • Knowledge of pharmaceutical analytical testing techniques • Hands‑on experience with HPLC and analytical laboratory instruments • Understanding of GLP and GMP regulatory guidelines • Experience with pharmaceutical documentation systems • Knowledge of IPQA operations in OSD manufacturing Candidates should be hardworking, dedicated, and capable of working within regulated pharmaceutical manufacturing environments. Location & Salary Job Location BioMatrix Healthcare Pvt. Ltd. Survey No. 624 Sarkhej‑Bavla Highway Village Rajoda Ahmedabad, Gujarat, India Ahmedabad is one of India’s major pharmaceutical manufacturing hubs and home to several global pharmaceutical companies and research organizations. Salary Salary packages for QC and QA roles depend on candidate experience, technical skills, and pharmaceutical industry exposure. Candidates working in regulated pharmaceutical environments may receive competitive compensation according to industry standards. Walk‑In Interview Details Interview Date 10 March 2026 (Tuesday) Registration Timing 09:00 AM to 01:00 PM Interview Venue BioMatrix Healthcare Pvt. Ltd. Survey No. 624 Sarkhej‑Bavla Highway Village Rajoda Ahmedabad, Gujarat Candidates attending the interview should bring: • Updated resume or CV • Educational qualification certificates • Experience documents (if applicable) • Identity proof Application Process Candidates who are unable to attend the walk‑in interview may submit their resume through email. Send your CV to: career@biomatrixhealthcare.com hr@biomatrixhealthcare.com Contact Numbers 63574 10551 63589 70525 97259 01031 92288 93058 Company Website www.biomatrixhealthcare.com Applicants are advised to mention their department experience and technical skills in pharmaceutical quality systems to improve chances of shortlisting. Why Build a Career with BioMatrix Healthcare Working in globally regulated pharmaceutical companies such as BioMatrix Healthcare allows professionals to gain exposure to international manufacturing standards, pharmaceutical regulatory systems, and advanced quality compliance frameworks. Quality control and quality assurance professionals play a crucial role in ensuring that medicines produced by pharmaceutical companies remain safe, effective, and compliant with international healthcare regulations. Professionals trained in these fields can build long‑term careers in areas such as: • Pharmaceutical Quality Assurance • Analytical Quality Control Laboratories • Regulatory Compliance Management • Pharmaceutical Manufacturing Operations • Global Regulatory Affairs Because pharmaceutical manufacturing must meet strict regulatory standards worldwide, professionals with expertise in GMP compliance, analytical testing, and pharmaceutical quality systems remain highly valuable within the global healthcare industry. Frequently Asked Questions (FAQs) Who can attend the BioMatrix Healthcare walk‑in interview? Candidates with MSc, BPharm, or MPharm qualifications and relevant pharmaceutical industry experience can attend the interview. Are freshers eligible for QC roles? Yes. Fresh graduates may apply for trainee roles in the Quality Control department. What analytical instruments should QC candidates know? Candidates should have knowledge of analytical instruments such as HPLC used in pharmaceutical analytical laboratories. What experience is required for QA positions? QA candidates should have experience in IPQA activities within OSD manufacturing processes such as granulation, compression, and coating. How can candidates apply if they cannot attend the interview? Candidates may send their updated CV to the official recruitment email addresses provided by BioMatrix Healthcare. Job Summary Company BioMatrix Healthcare Pvt. Ltd. Vacancies QC Trainee, QC Officer, QC Executive, QA Officer, QA Executive Required Education MSc Chemistry, MSc Analytical Chemistry, MSc Pharmaceutical Chemistry, BPharm, MPharm Experience 0–10 Years [...] Read more...

Certified HCC Medical Coders – Freshers SpyHealth Hiring | Hyderabad

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now SpyHealth RCM Announces Walk‑In Drive for HCC Coding Trainee Roles Fresh graduates exploring careers beyond traditional pharmacy and life science roles now have a new opportunity in healthcare analytics. SpyHealth RCM has announced a Direct Walk‑In Drive for HCC Coding Trainee positions, offering structured training, assessment, and placement support for candidates interested in medical coding careers. For B.Pharm, M.Pharm, life science, and even non‑life science graduates, this hiring program provides a pathway into the rapidly expanding healthcare revenue cycle management sector. With hospitals and insurance providers relying heavily on accurate clinical coding, trained HCC coders are becoming essential to modern healthcare systems. Company Overview SpyHealth RCM is a healthcare revenue cycle management and medical coding services organization supporting hospitals, healthcare providers, and insurance companies. The company focuses on medical coding, risk adjustment coding, healthcare documentation review, and clinical data management. Through structured training initiatives, SpyHealth RCM aims to build skilled medical coding professionals who can support healthcare organizations in maintaining accurate clinical records and compliant insurance documentation. The organization also provides practical training with real case scenarios, helping graduates develop industry‑relevant coding knowledge before entering professional roles in healthcare data services. Career Outlook for Safety Science & HCC Coding Analysts in 2026 Healthcare systems worldwide are moving toward data‑driven patient care and advanced risk adjustment models. By 2026, the demand for professionals skilled in Hierarchical Condition Category (HCC) coding, clinical documentation review, and healthcare analytics is expected to grow significantly. HCC coding professionals help healthcare providers analyze patient risk profiles, ensure accurate clinical documentation, and support insurance reimbursement models. Their work improves healthcare transparency, regulatory compliance, and data accuracy across hospitals and insurance platforms. Graduates who begin as HCC coding trainees often progress into roles such as Certified Medical Coder, Risk Adjustment Analyst, Coding Auditor, Clinical Documentation Specialist, or Healthcare Data Analyst. Job Role & Responsibilities The HCC Coding Trainee program is designed to train candidates in medical coding principles, clinical documentation interpretation, and risk adjustment coding systems used in healthcare analytics. Key responsibilities during and after training may include: Review clinical documentation and patient medical records Assign appropriate HCC and medical codes based on diagnoses Ensure accuracy in clinical coding and healthcare documentation Support healthcare data analysis for insurance and reimbursement processes Maintain coding compliance with healthcare regulations Collaborate with coding teams and healthcare documentation specialists Candidates will gain practical exposure through real‑time case discussions and structured training modules. Eligibility / Qualifications Candidates interested in the HCC coding trainee program should meet the following criteria: Graduate degree from Life Science or Non‑Life Science background Interest in medical coding, healthcare documentation, or healthcare analytics Basic understanding of human anatomy and medical terminology is beneficial Willingness to undergo structured training and assessment Relevant education backgrounds may include: B.Pharm, M.Pharm, Pharm.D, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Life Sciences, BPT, BMLT, B.Sc Nursing, BCA, B.Com, BA, and other graduate programs. Freshers looking to enter the healthcare IT and medical coding sector are encouraged to attend the walk‑in drive. Training Program Highlights The SpyHealth RCM program focuses on preparing graduates for real‑world medical coding roles. Program highlights include: Comprehensive HCC Coding training and assessment Real‑time learning through live case scenario discussions Hands‑on exposure to healthcare documentation review Placement support after successful completion of training This structured program helps candidates build practical industry skills before starting full‑time roles in healthcare coding operations. Walk‑In Details Candidates interested in the HCC Coding Trainee program can attend the direct walk‑in drive. Walk‑In Schedule: Dates: 9th – 13th march Time: 10:00 AM – 4:00 PM Contact Information: Email: hr@spyhealthrcm.com Website: www.spyhealthrcm.com Phone: +91 8374433746 / +91 7989578556 Candidates should bring updated resumes and educational documents when attending the walk‑in interview. Frequently Asked Questions Who can attend the SpyHealth medical coding walk‑in drive? Graduates from life science and non‑life science backgrounds who are interested in medical coding careers can attend. Is prior medical coding certification required? No. The program includes structured training designed for fresh graduates. What is HCC coding? HCC coding is a healthcare risk adjustment coding system used by insurance providers and healthcare organizations to assess patient conditions and treatment complexity. Will placement support be provided? Yes. Candidates completing the training and assessment program may receive placement support for medical coding roles. Summary Category Details Company SpyHealth RCM Vacancies HCC Coding Trainee Required Education B.Pharm, M.Pharm, Pharm.D, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Life Sciences, BPT, BMLT, BCA, B.Com, BA Experience Freshers Eligible Walk‑In Dates 9th – 13th Time 10:00 AM – 4:00 PM Program HCC Coding Training, Assessment, Placement Support [...] Read more...

Anthea walk‑in QA Officer & Executive

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BSc MSc QA Officer Walk‑In | Anthea Pharma Hyderabad BSc, MSc candidates – QA Officer & Executive walk‑in vacancies at Anthea Pharma USFDA sterile injectable facility Hyderabad. Anthea Pharma Pvt. Ltd. is conducting a walk‑in interview for Quality Assurance (QA) professionals at its USFDA‑approved sterile injectable manufacturing facility located in Hyderabad, Telangana. The company is inviting candidates with B.Sc or M.Sc qualifications and relevant pharmaceutical industry experience to join its growing quality assurance team. Quality assurance plays a critical role in pharmaceutical manufacturing by ensuring that medicines meet strict regulatory standards before reaching patients. QA professionals maintain compliance with Good Manufacturing Practices (GMP), manage quality management systems (QMS), and ensure that pharmaceutical products meet global regulatory expectations. This hiring opportunity is ideal for professionals who have experience working in regulated pharmaceutical environments, particularly in sterile injectable manufacturing, analytical documentation, and laboratory information management systems (LIMS). Selected candidates will work in a modern pharmaceutical facility that follows global compliance standards required by international healthcare regulators. Candidates who are ready to join immediately and are interested in working within a highly regulated pharmaceutical environment are encouraged to attend the walk‑in interview. Company Overview Anthea Pharma Pvt. Ltd. is a pharmaceutical manufacturing company specializing in sterile injectable formulations. The organization operates a USFDA‑approved manufacturing facility designed to produce high‑quality injectable medicines that meet global regulatory standards. Sterile injectable products are among the most critical forms of pharmaceutical therapy used in hospitals and healthcare institutions worldwide. Manufacturing such products requires highly controlled environments, advanced pharmaceutical technology, and strict adherence to Good Manufacturing Practices (GMP). Anthea Pharma has invested heavily in modern pharmaceutical manufacturing infrastructure, advanced laboratory systems, and strong quality management frameworks to ensure that its products meet international quality standards. The company’s Hyderabad facility supports pharmaceutical production, analytical testing, regulatory documentation, and quality compliance systems required for sterile injectable manufacturing. By joining Anthea Pharma, professionals gain exposure to globally regulated pharmaceutical manufacturing environments and advanced quality systems that support safe and effective medicine production. Job Role & Responsibilities The Quality Assurance team is responsible for maintaining compliance with pharmaceutical regulatory guidelines and ensuring that manufacturing processes meet strict quality standards. Quality Assurance Documentation QA professionals manage documentation systems that ensure pharmaceutical processes remain compliant with regulatory standards. Key responsibilities include: • Preparation of product specifications • Preparation of Standard Testing Procedures (STPs) • Creation and maintenance of analytical data sheets • Ensuring documentation complies with GMP guidelines Quality Management System (QMS) Quality management systems ensure pharmaceutical processes remain compliant and traceable. Key responsibilities include: • Handling QMS documentation and compliance activities • Supporting deviation management and investigation processes • Assisting with corrective and preventive actions (CAPA) • Maintaining documentation integrity and regulatory compliance Laboratory Information Management System (LIMS) QA professionals work with digital laboratory systems used to manage analytical data and quality records. Key responsibilities include: • Master data creation in LIMS • Maintaining laboratory data records • Ensuring analytical data accuracy and traceability Pharmacopoeia Updates & Compliance Senior QA professionals also ensure that analytical methods follow updated regulatory guidelines. Responsibilities include: • Monitoring pharmacopoeia updates • Ensuring laboratory methods remain compliant with regulatory requirements • Supporting analytical documentation updates These activities ensure pharmaceutical products are manufactured according to internationally accepted quality standards. Eligibility / Qualifications Candidates applying for the Quality Assurance roles must have relevant academic qualifications in science disciplines and experience working in pharmaceutical environments. Required Educational Background BSc Chemistry, BSc Life Sciences, BSc Biotechnology, MSc Chemistry, MSc Analytical Chemistry, MSc Biotechnology, MSc Life Sciences Candidates with strong knowledge of pharmaceutical documentation systems and regulatory compliance practices will be preferred. Experience Requirements Officer / Junior Officer 1 to 2 Years Executive 3 to 6 Years Experience in pharmaceutical quality assurance, documentation management, and GMP‑compliant manufacturing environments will be advantageous. Required Skills The ideal candidate should demonstrate: • Knowledge of pharmaceutical quality assurance systems • Experience in preparing specifications and STPs • Familiarity with LIMS data management systems • Understanding of QMS activities • Awareness of pharmacopoeia updates and regulatory guidelines Male candidates who can join immediately may receive preference according to company hiring requirements. Location & Salary Job Location Anthea Pharma Pvt. Ltd. USFDA Approved Sterile Injectable Facility Plot No. 290, Sy. No. 219 & 183 Pashamylaram Patancheru Mandal Sangareddy District Hyderabad, Telangana – 502307 Hyderabad is one of India’s largest pharmaceutical manufacturing hubs and home to several global pharmaceutical companies, research organizations, and biotechnology firms. Salary Salary packages for QA officers and executives typically depend on experience, regulatory exposure, and technical skills. Candidates with experience in sterile pharmaceutical manufacturing environments may receive competitive industry compensation. Employee Benefits Anthea Pharma provides several employee benefits including: • Subsidized canteen facility • Transportation support for employees These benefits support employee convenience and workplace comfort. Walk‑In Interview Details Interview Date 10 March 2026 Interview Timing 10:00 AM to 12:00 PM Candidates attending the interview should carry: • Updated resume • Educational certificates • Experience documents • Identity proof Candidates who are ready to join immediately are strongly encouraged to attend the interview. Application Process Candidates who cannot attend the walk‑in interview may send their updated CV through email. Send your resume to: recruitment@antheapharma.com Company Website www.antheapharma.com Contact Number 08455 696000 Applicants should clearly mention their experience in pharmaceutical quality assurance and documentation systems within their resume for better shortlisting. Why Build a Career in Pharmaceutical Quality Assurance Quality assurance is one of the most critical departments in pharmaceutical manufacturing because it ensures that medicines meet strict safety and quality standards before reaching patients. QA professionals work closely with production teams, analytical laboratories, and regulatory specialists to maintain compliance with international pharmaceutical regulations. Professionals trained in pharmaceutical quality systems gain valuable expertise in GMP compliance, documentation integrity, regulatory inspections, and pharmaceutical risk management. These skills open career opportunities in global pharmaceutical companies and biotechnology organizations. Typical career progression may include: • QA Officer • Senior QA Executive • Quality Compliance Manager • Pharmaceutical Regulatory Affairs Specialist • Quality Systems Manager Because regulatory compliance is essential in pharmaceutical manufacturing, experienced QA professionals remain in high demand worldwide. Frequently Asked Questions (FAQs) Who can attend the Anthea Pharma QA walk‑in interview? Candidates with BSc or MSc qualifications and 1–6 years of pharmaceutical QA experience can attend the interview. What skills are required for QA roles at Anthea Pharma? Candidates should have experience in preparing specifications, STPs, handling QMS documentation, and managing laboratory data within LIMS systems. Where is the job location? The role is based at Anthea Pharma’s USFDA‑approved sterile injectable manufacturing facility in Hyderabad, Telangana. Can candidates apply by email? Yes. Candidates who cannot attend the walk‑in interview may send their updated resume to the official recruitment email provided by the company. What benefits are provided by the company? Employees receive benefits such as subsidized canteen services and transportation facilities. Job Summary Company Anthea Pharma Pvt. Ltd. Vacancies QA Officer, QA Jr Officer, QA Executive Required Education BSc Chemistry, BSc Life Sciences, BSc Biotechnology, MSc Chemistry, MSc Analytical Chemistry, MSc Biotechnology Experience 1–6 Years [...] Read more...

Hetero Pharma Campus Placement Drive at Jayamukhi College of Pharmacy

July 19, 2024WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Jayamukhi College of Pharmacy, located in Chennaraopet Mandal, Narsampet (RM), Warangal (Dist.), is excited to announce a campus placement drive by Hetero Pharma on July 29, 2024. This event is a fantastic opportunity for B. Pharmacy and M. Pharmacy graduates to secure positions in Quality Control (QC) and Research & Development (R&D) with attractive salary packages. Event Details Date & Time: 29 July, 2024 @ 9:30 AM Venue: Jayamukhi College of Pharmacy, Chennaraopet Mandal, Narsampet (RM), Warangal (Dist.) Eligibility Criteria Education Qualification: B. Pharmacy with 1st Class M. Pharmacy with 1st Class Positions Offered 1. Quality Control (QC) For: B. Pharmacy Graduates Salary: LPA: 2.87 2. Research & Development (R&D) For: M. Pharmacy Graduates Salary: LPA: 3.10 How to Register Interested candidates can register for the placement drive by Registration Link contacting the following numbers for more information: +919989942346 +919381874572 +919949424160 [...] Read more...

NIPERG Vacancy for Junior Research Fellow (MS/ M Pharm / MSc) in Pharmacology

June 27, 2024WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now NIPERG JRF Recruitment The National Institute of Pharmaceutical Education & Research, Guwahati (NIPERG), is seeking applications for a Junior Research Fellow (JRF) in Pharmacology. This esteemed institution, established by the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers, Govt. of India, aims to fill this position under a DST-SERB sponsored project. Qualified candidates with MS, M Pharm, or MSc in Pharmacology are invited to apply by 30th June 2024. Job Details Position: Junior Research Fellow (JRF) Fellowship: ₹31,000/- plus 16% HRA Number of Positions: 1 Project: DST-SERB sponsored project entitled “Evaluating the role of SERCA activation in febrile seizure and its relationship with proinflammatory cytokine release” (GAP-150) Location: NIPER Guwahati, Assam, India Qualifications and Experience Essential: Postgraduate degree (MS/M Pharm/MSc) in Pharmacology from a PCI/AICTE/UGC/NAAC recognized/accredited University/Institute with a minimum of 60% marks. Cleared GPAT/GATE/CSIR-NET or any National entrance test exam conducted by any Central Govt. agency. Desirable: Experience in animal handling, neurobehavioral assessments, in-vitro cell culture techniques, and molecular biology techniques (Western blot, ELISA, qRT-PCR, Flowcytometer). Age Limit: 30 years (Age relaxation as per GoI norms) Responsibilities Conduct research on the DST-SERB sponsored project focused on SERCA activation and its effects on febrile seizures. Perform experimental tasks related to neurobehavioral assessments and molecular biology techniques. Maintain detailed documentation and present findings at various stages of the project. Application Process Application Period: 24th June 2024 – 30th June 2024 Application Method: Online applications only through NIPER Guwahati’s website. General Instructions Candidates of Indian Nationality can only apply. Interested candidates are invited to apply using the prescribed format only, available on the website (www.niperguwahati.ac.in) from 24.06.2024 to 30.06.2024. It is mandatory to fill the application online and no other form of application will be entertained. Candidates are requested to arrange the softcopies of all the required documents before filling the application. Candidates should read carefully the requisite minimum essential qualifications, age and eligibility, experience criteria etc. laid down in the advertisement before applying for the above post. Since all the applications will be screened on the basis of data submitted by the candidate in the online application form, the candidates must satisfy themselves of the suitability for the position to which they are applying. If at any stage during the recruitment and selection process, it is found that candidates have furnished false or wrong information, their candidature will be rejected. Application once submitted cannot be altered / resubmitted, under any circumstances. Further, no request with respect to making changes in any data/ particular entered by the candidate in the application will be entertained, once the application is submitted successfully by Email. Incomplete application or those without relevant supporting documents (self-attested copies of Date of birth/Degrees/ Certificates/ Mark sheets/Experience Certificates/documents, etc.) will be rejected. On the recommendation of the Screening/Selection Committee, the competent authority may relax all or any of the requirements related to age and experience in exceptionally meritorious cases. Fulfillment of qualifications and experience is an essential requirement. As stated, the Institute is free to set the benchmark and call only the eligible candidates for physical/ on-line interview. Further, NIPER Guwahati also reserves the right NOT to fill any of the post advertised, in the event or exigency so decided. Intimations will be sent only by E-mail/host on the website as per the details mentioned in the Application form. In case any dispute arises on account of interpretation of clauses in any version of this Advertisement other than English, the English version available on the NIPER-G Website shall prevail. CANVASSING IN ANY FORM MAY LEAD TO CANCELLATION OF THE CANDIDATE. The project tenure is upto the month of September 2024. The appointment is against the temporary project positions and will not continue in any circumstances beyond the duration of the said project. Any subsequent contract in the project or another project will be fresh appointment. The appointment in the outside funded project does not give project staff any claim whatsoever for appointment/regularization against any Institute post. Age will be calculated as on the last date of application i.e. 30.06.2024. List of the Shortlisted candidates will be displayed on the Institute website. The date and time of the interview will be communicated to the shortlisted candidates only. In-case of online interviews only, the link for the online interviews will be sent to the shortlisted candidates individually, a day before the interview. Full detailed Notification click here [...] Read more...

Pfizer Hiring Diploma Pharmacy Freshers 2025 | Junior Associates | Vizag

October 24, 2025WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Diploma Pharmacy Freshers 2025 | Junior Associates at Pfizer Vizag Pfizer Healthcare India is hiring 2025 Diploma Pharmacy Freshers for Junior Associate roles in Vizag. 30 openings available. Apply now! Pfizer Healthcare India Private Limited, a global leader in pharmaceuticals, is offering an excellent opportunity for Diploma Pharmacy Freshers (2025 batch) to kickstart their careers as Junior Associates – Manufacturing at its Vizag facility. This position is ideal for candidates who want to begin their journey with one of the world’s most respected pharma brands, gaining valuable hands-on experience in a world-class production environment. Company Overview Pfizer Healthcare India Pvt. Ltd., headquartered in Mumbai with a major manufacturing facility in Visakhapatnam (Vizag), is a subsidiary of Pfizer Inc., USA — one of the world’s leading biopharmaceutical companies. The Vizag site specializes in sterile injectable manufacturing, ensuring global compliance and innovation in life-saving drug production. Pfizer’s manufacturing excellence, coupled with cutting-edge technology, provides young professionals an incredible platform to learn about Good Manufacturing Practices (GMP), pharma production standards, and regulatory compliance under expert supervision. Job Role & Responsibilities As a Junior Associate in Manufacturing, your key responsibilities include: Operating advanced production and formulation equipment including injectable, parenteral, sterile, filling, and capping machines. Monitoring production parameters and ensuring products meet Pfizer’s high-quality standards. Performing preventive maintenance and troubleshooting minor machine issues. Maintaining accurate records and documentation as per cGMP and SOP guidelines. Participating in continuous improvement activities to optimize plant efficiency. Ensuring compliance with all safety, hygiene, and quality protocols. This role offers freshers a hands-on introduction to pharmaceutical manufacturing operations, providing strong foundational exposure in one of India’s most advanced pharma facilities. Eligibility / Qualifications To be eligible for this role, candidates must meet the following criteria: Qualification: Diploma in Pharmacy (D.Pharm) Batch: 2025 Pass-outs only Academic Requirement: Minimum 60% aggregate with no active backlogs Experience: 0–1 year (Freshers preferred) Core Skills: Technical aptitude, understanding of basic pharma operations, teamwork, communication skills Preferred Courses for Eligibility: D.Pharm, Diploma in Pharmaceutical Sciences, Diploma in Drug Technology, Diploma in Industrial Pharmacy Pfizer strongly values candidates with a positive learning attitude, strong discipline, and a passion for contributing to healthcare innovation. Location & Salary Location: Visakhapatnam, Andhra Pradesh, India Work Type: Full-time, Permanent Industry: Pharmaceutical & Life Sciences Department: Production, Manufacturing & Engineering Role Category: Operations, Maintenance & Support Salary: Not Disclosed (Competitive pay and benefits offered as per Pfizer’s HR policies) Pfizer offers an inclusive work environment with structured training, mentorship, and opportunities for internal career progression. Application Process Interested candidates can apply online through the official Naukri job link below: 👉 Apply Here on Naukri Note: Applications are open for a limited time. Freshers meeting the criteria are encouraged to apply early to secure their interview slot. Why Join Pfizer Healthcare India? Work with a global leader in pharmaceutical manufacturing Gain hands-on experience with world-class production systems Exposure to sterile injectable and parenteral manufacturing Learn and grow under industry experts Attractive career progression opportunities within Pfizer Opportunity to work on life-saving products impacting global healthcare This is not just a job — it’s a career launchpad with one of the most reputable pharma companies globally. FAQs 1. Who can apply for Pfizer’s Diploma Pharmacy Fresher role? Only candidates from the 2025 batch with a Diploma in Pharmacy and at least 60% aggregate marks can apply. 2. Is this opportunity available for B.Pharm or M.Pharm graduates? No, this particular opening is strictly for Diploma Pharmacy (D.Pharm) candidates. 3. What is the job location? The role is based in Visakhapatnam (Vizag), Andhra Pradesh. 4. Is prior experience required? No. This position is for fresh graduates (0–1 year experience) looking to start their pharma manufacturing career. 5. What is the last date to apply? Pfizer has not specified a closing date, but candidates are advised to apply as soon as possible since the openings are limited. 6. What is the selection process? Shortlisted candidates will go through screening, followed by a technical and HR interview. 7. What is the expected salary for freshers? Pfizer offers competitive compensation, training benefits, and career development opportunities. Salary is based on company standards and role requirements. Company Pfizer Healthcare India Pvt. Ltd. Vacancies 30 Required Education Diploma in Pharmacy (D.Pharm), Diploma in Pharmaceutical Sciences, Diploma in Drug Technology Experience 0–1 Year (Freshers 2025 Batch) [...] Read more...

NIPER Kolkata Recruitment for Professor, Associate Professor & Non-Teaching posts

December 15, 2025WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now NIPER Kolkata Recruitment 2025 | Pharma Faculty & Admin Jobs NIPER Kolkata invites applications for Professor, Associate Professor & Non-Teaching posts. Pharma faculty & admin vacancies in Kolkata. National Institute of Pharmaceutical Education and Research (NIPER), Kolkata has released its official Recruitment Notification 2025 for Teaching and Non-Teaching positions on a direct recruitment and deputation basis. NIPER Kolkata, an Institute of National Importance under the Department of Pharmaceuticals, Government of India, offers highly prestigious academic and administrative career opportunities with central government pay scales, allowances, and long-term job stability. This recruitment drive is open to eligible Indian nationals across pharmaceutical sciences, academic research, and administration domains through an all-India level selection process. fileciteturn0file0 Company Overview The National Institute of Pharmaceutical Education and Research (NIPER), Kolkata was established in 2007 by an Act of Parliament and functions under the Ministry of Chemicals and Fertilizers, Government of India. NIPERs are apex institutions dedicated to advanced education, research, and innovation in pharmaceutical sciences, regulatory science, and allied healthcare disciplines. NIPER Kolkata plays a critical role in strengthening India’s pharmaceutical education ecosystem by producing high-quality faculty, researchers, and administrators who contribute directly to drug discovery, regulatory compliance, pharmaceutical manufacturing, and public health advancement. fileciteturn0file0 Job Role & Responsibilities Teaching Positions Professor – Medicinal Chemistry (Pay Level 14, 7th CPC) Lead advanced teaching and research activities in medicinal chemistry Supervise PhD and postgraduate research scholars Conduct independent, high-impact research in drug discovery and allied areas Publish in high-quality SCI/SCOPUS-indexed journals Establish computational and experimental research facilities Collaborate with interdisciplinary research teams Associate Professor – Pharmaceutical Analysis (Pay Level 13, 7th CPC) Deliver postgraduate and doctoral-level teaching Conduct research in pharmaceutical and bio-analytical sciences Guide MSc, MPharm, and PhD students Handle advanced analytical instruments (HPLC, LC-MS/MS, GC-MS) Support regulatory, quality, and compliance-driven research Non-Teaching Positions Finance & Accounts Officer (Pay Level 12, 7th CPC) Manage finance, budgeting, audit, and accounting functions Ensure compliance with central government financial rules Handle accounting software and institutional finance systems Estate & Security Officer (Pay Level 10, 7th CPC) Oversee campus security, estate management, and infrastructure Coordinate civil, electrical, and security operations Public Relations Officer (Pay Level 8, 7th CPC) Manage institutional communications and public relations Coordinate media, events, placements, and outreach activities Eligibility / Qualifications Teaching Posts – Educational Requirements PhD with first-class academic record in relevant pharmaceutical disciplines Significant teaching, research, or industrial experience Strong publication record in SCI/SCOPUS journals Relevant academic specializations include: Medicinal Chemistry, Pharmaceutical Analysis, Pharmacology, Pharmaceutics, Pharmacognosy, Pharmaceutical Biotechnology, Regulatory Toxicology, Clinical Pharmacy, Pharmacoinformatics Non-Teaching Posts – Educational Requirements Postgraduate degree in Commerce, Economics, Administration, or relevant discipline Relevant government or autonomous institutional experience Age limits, experience criteria, and reservation rules are strictly as per Government of India norms. fileciteturn0file0 Location & Salary Job Location: Kolkata, West Bengal Pay Scale: As per 7th Central Pay Commission Benefits: DA, HRA, Transport Allowance, Medical reimbursement, LTC, Pension under NPS Application Process Candidates must apply online only through the official NIPER Kolkata recruitment portals. Online Application Start Date: 10 December 2025 Last Date to Apply Online: 09 January 2026 Last Date for Hard Copy Submission: 23 January 2026 Apply Links: Teaching Posts: https://niperkrecruitment.in/teaching Non-Teaching Posts: https://niperkrecruitment.in/nonteaching/ All shortlisted candidates will be notified via email for seminar presentations, written tests, and interviews as applicable. fileciteturn0file0 Why Join NIPER Kolkata Central Government job with long-term stability Prestigious academic and research environment High-impact contribution to pharmaceutical education and research Competitive 7th CPC pay scales and allowances Opportunities for sponsored research, consultancy, and innovation FAQs Who can apply for NIPER Kolkata Recruitment 2025? Eligible Indian nationals meeting qualification, age, and experience criteria. Are these permanent government jobs? Yes. Direct recruitment posts are regular with probation as per rules. Is deputation option available? Yes, for selected teaching and non-teaching positions. What is the selection process? Teaching posts involve seminar presentation and interview. Non-teaching posts involve written test, skill test, and interview. Where can I find official notification details? On the official NIPER Kolkata website and recruitment portals. Company NIPER Kolkata Vacancies Teaching & Non-Teaching Required Education PhD / PG / Relevant Discipline Experience As per post [...] Read more...

CSIR–CDRI Project Associate Recruitment 2026

February 7, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now CSIR–Central Drug Research Institute (CDRI), Lucknow, is inviting online applications for Project Associate-I and Project Associate-II positions under the BMGF-funded research project on Long Acting Injectables (LAIs) for Tuberculosis. A total of three project vacancies are available, including two openings for Project Associate-I and one opening for Project Associate-II. These positions are part of the pharmaceutical research and formulation development team and are ideal for M.Pharm or MS (Pharm) candidates with GPAT qualification. The engagement is purely temporary, project-based, and based at CSIR-CDRI, Lucknow. Company Overview CSIR–Central Drug Research Institute (CDRI), Lucknow, is one of India’s premier national laboratories under the Council of Scientific and Industrial Research (CSIR). The institute is internationally recognized for its contribution to drug discovery, pharmaceutical research, and translational science. CSIR-CDRI has played a pivotal role in the development of several indigenous drugs, diagnostics, and healthcare solutions that have had a direct impact on public health. The institute collaborates with global funding agencies, academic institutions, and industry partners to address critical healthcare challenges. The current recruitment is under a prestigious Bill & Melinda Gates Foundation (BMGF) funded project focused on the development of long acting injectable formulations for tuberculosis, a high-priority global health area. Working at CSIR-CDRI offers researchers exposure to advanced analytical techniques, regulatory-aligned research practices, and multidisciplinary scientific environments. Job Role & Responsibilities The Project Associate roles are research-intensive positions supporting formulation development and preclinical research activities under the BMGF project. Selected candidates will work closely with principal investigators and senior scientists on laboratory-based experimental work and documentation. Key Responsibilities Supporting formulation development activities related to long acting injectable drug delivery systems Performing analytical testing using HPLC and LC-MS techniques Assisting in method development, validation, and data interpretation Handling laboratory documentation and maintaining experimental records Supporting animal handling activities as per approved protocols Participating in sample preparation, stability studies, and data compilation Assisting in preparation of project reports and research documentation Following laboratory safety guidelines and institutional research protocols Position-wise Role Scope Project Associate-I: Entry-level research support role focused on laboratory execution and data generation Project Associate-II: Advanced research role involving independent experimental work and mentoring junior staff These roles directly contribute to translational pharmaceutical research aimed at improving tuberculosis treatment outcomes. Eligibility / Qualifications Educational Qualification M.Pharm or MS (Pharm) GPAT qualification is mandatory for both positions Experience Requirement Project Associate-I: Fresh postgraduates or candidates with limited research exposure Project Associate-II: Minimum 2 years of relevant research experience Desirable Skills and Experience Hands-on experience with HPLC and LC-MS instruments Exposure to formulation development techniques Experience in animal handling and preclinical studies Familiarity with pharmaceutical research documentation Eligible Courses (Comma-Separated) M.Pharm, MS (Pharm), M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Analysis, M.Pharm Industrial Pharmacy Location & Salary Job Location CSIR–Central Drug Research Institute, Lucknow, Uttar Pradesh, India Monthly Emoluments Project Associate-I: Rs. 31,000 + 20% HRA per month Project Associate-II: Rs. 35,000 + 20% HRA per month Age Limit Maximum 35 years as on the last date of application The positions are temporary and co-terminus with the project. Initial engagement is for one year and extendable based on performance and project requirements. Application Process Eligible candidates must apply online through the official CSIR-CDRI recruitment portal. No hard copy of the application is required at the time of submission. How to Apply Apply online using the official link below: https://cdri.res.in/032026/ Important application details: Online application start date: 06 February 2026 (10:00 AM) Last date to apply: 16 February 2026 (11:59 PM) Applications must be submitted using a desktop or laptop only Communication regarding selection will be sent to the registered email ID Candidates shortlisted for interview must bring a printed copy of the application along with original certificates and testimonials at the time of joining. FAQs How many vacancies are available under this recruitment? There are three project vacancies: two for Project Associate-I and one for Project Associate-II. Is GPAT qualification mandatory? Yes. GPAT qualification is mandatory for both Project Associate-I and Project Associate-II positions. Are these permanent jobs? No. These are purely temporary, project-based positions co-terminus with the project duration. What is the age limit for applying? The upper age limit is 35 years. Age relaxation may be applicable as per Government of India rules. Can candidates apply for more than one post? Yes. Eligible candidates may apply for multiple project posts. Summary Table Company CSIR–Central Drug Research Institute (CDRI), Lucknow Vacancies Project Associate-I (02), Project Associate-II (01) Required Education M.Pharm, MS (Pharm), GPAT Qualified Experience Fresher (PA-I), 2 Years (PA-II) [...] Read more...

OPES Healthcare Walk‑In QA, ADL, F&D, Packaging

March 7, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BPharm MSc Pharma Vacancies Walk‑In | OPES Healthcare Ahmedabad BPharm, MPharm, MSc pharma walk‑in vacancies across QA, ADL, F&D, Packaging at OPES Healthcare Ahmedabad. Multiple positions available. OPES Healthcare is conducting a walk‑in interview to hire experienced pharmaceutical professionals across multiple departments including Quality Assurance (QMS), Formulation & Development (Sterile), Analytical Development Laboratory (ADL), Packaging Operations, and Packaging Development Cell (PDC). The recruitment drive is open to candidates from pharmaceutical formulation backgrounds who are looking to work in regulated manufacturing and pharmaceutical product development environments. This hiring initiative is aimed at strengthening OPES Healthcare’s quality systems, analytical development capabilities, sterile product formulation research, and packaging innovation functions. Professionals selected through this recruitment process will contribute directly to ensuring pharmaceutical product quality, regulatory compliance, and safe drug delivery systems. The walk‑in interview provides an opportunity for experienced candidates in pharmaceutical manufacturing, analytical testing, quality management systems, and sterile product development to join a fast‑growing healthcare organization with modern pharmaceutical operations. Company Overview OPES Healthcare is a pharmaceutical company focused on delivering high‑quality healthcare solutions through strong manufacturing practices, regulatory compliance systems, and innovative product development. The company supports the pharmaceutical ecosystem by developing and manufacturing pharmaceutical formulations that meet strict quality and regulatory standards required by global healthcare markets. The organization emphasizes strong quality assurance systems, robust analytical testing infrastructure, and continuous innovation in pharmaceutical formulation and packaging technologies. These functions ensure that medicines produced by the company maintain safety, stability, and therapeutic effectiveness. Operating from Ahmedabad, Gujarat—one of India’s major pharmaceutical manufacturing clusters—OPES Healthcare collaborates with pharmaceutical experts, formulation scientists, analytical chemists, and quality assurance professionals to deliver compliant and high‑quality healthcare products. The company also offers a supportive work environment with structured HR policies, employee health benefits, and professional growth opportunities for pharmaceutical professionals. Job Role & Responsibilities OPES Healthcare is hiring for multiple pharmaceutical departments. Each role plays an important part in maintaining product quality, supporting pharmaceutical development, and ensuring regulatory compliance. Quality Assurance – QMS Quality Assurance professionals ensure that pharmaceutical manufacturing operations comply with regulatory guidelines such as GMP and global pharmaceutical quality standards. Key responsibilities include: • Managing Quality Management System (QMS) documentation • Monitoring compliance with Good Manufacturing Practices (GMP) • Reviewing batch manufacturing records and quality documentation • Supporting internal quality audits and regulatory inspections • Implementing corrective and preventive action systems (CAPA) • Ensuring data integrity and regulatory documentation compliance Formulation & Development (Sterile) F&D professionals work on development and optimization of sterile pharmaceutical formulations. Key responsibilities include: • Developing sterile pharmaceutical formulations • Conducting formulation trials and stability studies • Supporting scale‑up and technology transfer activities • Monitoring product stability and formulation performance • Ensuring compliance with sterile manufacturing guidelines Analytical Development Laboratory (ADL) ADL scientists perform analytical testing and method development to support pharmaceutical product quality and stability. Key responsibilities include: • Performing analytical testing of pharmaceutical samples • Conducting method development and method validation • Performing stability testing and impurity profiling • Using chromatography and spectroscopy techniques • Supporting regulatory documentation and analytical reports Packaging Department Packaging professionals ensure safe, compliant, and efficient pharmaceutical product packaging operations. Key responsibilities include: • Monitoring packaging line operations • Ensuring packaging quality and compliance standards • Reviewing packaging batch records • Supporting packaging validation activities • Maintaining packaging documentation and compliance records Packaging Development Cell (PDC) Packaging development specialists design and evaluate packaging solutions for pharmaceutical products. Key responsibilities include: • Developing innovative pharmaceutical packaging systems • Conducting packaging compatibility studies • Evaluating packaging materials and stability • Supporting packaging validation and regulatory documentation • Ensuring packaging integrity for drug safety Eligibility / Qualifications Candidates applying for these positions must have academic qualifications in pharmaceutical sciences or related life sciences disciplines. Required Educational Background B.Pharm, M.Pharm, B.Sc Chemistry, B.Sc Pharmaceutical Sciences, M.Sc Chemistry, M.Sc Analytical Chemistry, D.Pharm, Diploma in Packaging Technology Only candidates with pharmaceutical formulation industry experience will be considered for these roles. Experience Requirements QA (QMS) 5 to 7 Years F&D (Sterile) 8 to 12 Years Analytical Development Laboratory (ADL) 2 to 7 Years Packaging Department 2 to 5 Years Packaging Development Cell (PDC) 5 to 7 Years Candidates with strong knowledge of pharmaceutical regulatory guidelines, GMP compliance, and formulation manufacturing systems will be preferred. Location & Salary Interview & Office Location OPES Healthcare 3rd Floor, Tulsi Plaza Opposite Ginger Hotel Sarkhej‑Bavla Road Changodar, Ahmedabad – 382213 Gujarat, India Ahmedabad is one of India’s largest pharmaceutical manufacturing hubs and provides strong career opportunities for professionals in formulation development, analytical testing, and pharmaceutical quality systems. Salary Compensation for these roles will depend on candidate experience, technical expertise, and previous pharmaceutical industry exposure. Competitive salary packages and employee benefits will be offered according to company HR policies. Employee Benefits OPES Healthcare offers several employee‑focused benefits including: • Employee health insurance policy • Accidental insurance coverage • Air‑conditioned transportation facility • Attractive HR policies and workplace benefits • Second and fourth Saturday off These benefits are designed to support employee well‑being and maintain a balanced professional work environment. Walk‑In Interview Details Interview Date 08 March 2026 Interview Time 9:00 AM to 2:00 PM Candidates attending the interview should bring the following documents: • Updated resume • Last three months salary slips • Educational qualification certificates • Identity proof Application Process Candidates who are unable to attend the walk‑in interview may submit their resume through email. Send your CV to: career@opeshealthcare.com Contact Numbers 85118 49377 74868 29377 Company Website www.opeshealthcare.com Applicants should clearly mention their department experience and pharmaceutical formulation background in their resume for better shortlisting. Why Work in Pharmaceutical Quality, R&D, and Packaging Pharmaceutical manufacturing relies heavily on specialized professionals across quality assurance, analytical laboratories, formulation development, and packaging innovation. These departments ensure that medicines meet strict regulatory requirements and remain safe for patient use. Professionals working in these roles gain expertise in pharmaceutical manufacturing processes, regulatory compliance systems, analytical technologies, and drug delivery packaging solutions. Such experience opens opportunities for career growth across global pharmaceutical companies and biotechnology organizations. Common career growth paths include: • Quality Assurance Manager • Formulation Development Scientist • Analytical Research Scientist • Packaging Technology Specialist • Pharmaceutical Regulatory Compliance Manager Because pharmaceutical products must meet strict global regulatory standards, skilled professionals in quality systems, analytical testing, and formulation development remain highly valuable within the healthcare industry. Frequently Asked Questions (FAQs) Who can attend the OPES Healthcare walk‑in interview? Candidates with B.Pharm, M.Pharm, B.Sc, M.Sc, D.Pharm, or Packaging Technology qualifications and pharmaceutical formulation industry experience can attend. Is pharmaceutical formulation experience mandatory? Yes. Only candidates with pharmaceutical formulation industry backgrounds will be considered. What departments are hiring in this recruitment drive? The company is hiring for Quality Assurance (QMS), Formulation & Development (Sterile), Analytical Development Laboratory (ADL), Packaging, and Packaging Development Cell. Can candidates apply through email instead of attending the walk‑in? Yes. Candidates can send their updated CV directly to the official recruitment email provided by OPES Healthcare. Where is the interview location? The walk‑in interview will take place at OPES Healthcare’s office in Changodar, Ahmedabad, Gujarat. Job Summary Company OPES Healthcare Vacancies QA Executive, QA Sr Executive, F&D Sterile Manager, ADL Officer, ADL Sr Executive, Packaging Officer, Packaging Executive, Packaging Development Sr Executive Required Education BPharm, MPharm, BSc Chemistry, MSc Chemistry, MSc Analytical Chemistry, DPharm, Diploma in Packaging Technology Experience 2–12 Years depending on department [...] Read more...

Fresher Jobs

Labcorp Hiring Data Management Associate I (Entry Level)

March 14, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Labcorp Hiring Data Management Associate I – Clinical Data Management Jobs in Bangalore (Entry Level) Labcorp is inviting applications for the role of Data Management Associate I in its Global Data Management Solutions group located at Brigade Twin Towers, Bangalore, India. This is an entry-level clinical data management opportunity, making it ideal for fresh graduates in life sciences, statistics, computer science, mathematics, or related disciplines who are looking to begin a career in the clinical research and pharmaceutical data management industry. The role involves learning and supporting database-related activities for nonclinical and research studies, including data compilation, database population, metadata management, and quality checking of study datasets. Candidates interested in clinical data management, clinical research data analytics, and pharmaceutical database operations will find this position an excellent starting point for building long-term careers in the global CRO and life sciences industry. This position is based in Bangalore, Karnataka, and follows a PM shift schedule (2:00 PM – 11:00 PM) within Labcorp’s global operations team. Company Overview Labcorp is a global life sciences company that provides comprehensive clinical research, laboratory testing, and drug development services to pharmaceutical, biotechnology, and healthcare organizations worldwide. The company plays a critical role in supporting clinical trials, medical diagnostics, drug safety monitoring, and healthcare research that improve patient outcomes globally. With operations across more than 100 countries, Labcorp collaborates with pharmaceutical sponsors and healthcare providers to accelerate drug development and deliver innovative medical solutions. The organization offers services ranging from clinical development and central laboratory services to real-world data analytics and diagnostic testing. Labcorp’s data management teams support global research programs by ensuring the accurate collection, validation, and management of scientific data generated during research and development studies. Employees working at Labcorp benefit from exposure to global clinical research operations, advanced data systems, and a collaborative work culture focused on improving human health through science and innovation. Job Role and Responsibilities The Data Management Associate I works within the global data management solutions group and supports database-related activities used in nonclinical studies and research projects. The role focuses on learning the processes involved in clinical research data management, database population, and data validation workflows. Database Management Responsibilities • Learn how to review study documents such as protocols and research reports to extract relevant data for database entry • Compile metadata required to populate internal research databases • Assist in preparing and generating database requests for research studies • Perform quality checks on compiled datasets before database submission • Convert manually compiled data, often from spreadsheets, into formats suitable for database systems • Generate information searches to identify relevant study data within required timelines Software and Data Tools • Use software tools such as Microsoft Word, Excel, and database management applications to support daily tasks • Work with collaboration and document-sharing platforms used within research teams • Generate tables, datasets, and spreadsheets for reporting purposes • Learn database systems used in clinical and nonclinical research data management Software Testing and Validation • Participate in training related to software testing and validation procedures used within research data systems • Execute test scripts as part of the Systems Life Cycle (SLC) methodology • Maintain documentation supporting software validation in accordance with regulatory standards Communication and Client Support • Learn to communicate with internal and external clients regarding database requests • Assist in preparing communication templates and form letters related to project workflows • Collaborate with project teams to ensure accurate data handling and reporting Additional Responsibilities • Support ongoing research projects and data management initiatives • Assist senior data management staff with project-related tasks • Maintain proper documentation for database requests and data handling processes • Perform additional duties as assigned by project managers or supervisors Through these responsibilities, the Data Management Associate contributes to the accurate management of research data that supports scientific analysis, regulatory documentation, and clinical development programs. Eligibility and Qualifications Candidates interested in applying for the Data Management Associate I role at Labcorp should meet the following educational and skill requirements. Educational Qualification Bachelor’s degree or equivalent experience in relevant disciplines. Relevant educational backgrounds include: BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Statistics, BSc Mathematics, BSc Computer Science, BSc Information Systems, BCA, BTech Biotechnology, BTech Computer Science. Experience This is an entry-level role, making it suitable for fresh graduates or candidates with minimal experience who are interested in starting careers in clinical data management or research data operations. Technical Skills • Basic knowledge of Microsoft Office tools such as Excel, Word, and Adobe Acrobat • Understanding of spreadsheet data handling and documentation practices • Familiarity with research databases or data analysis tools is an advantage • Knowledge of programming or statistical tools such as SAS, R, or Python is preferred but not mandatory • Ability to learn database and clinical research data management systems quickly Professional Skills • Strong attention to detail and accuracy when working with research datasets • Good time management and organizational abilities • Strong communication skills for working with global teams • Ability to work collaboratively within project teams • Analytical thinking and problem-solving skills Graduates interested in careers in clinical data management, research data analysis, and pharmaceutical data science will find this role highly suitable as an entry point into the global life sciences industry. Location and Salary Location: Bangalore, Karnataka, India Work Schedule: PM Shift (2:00 PM – 11:00 PM) Work Environment: Office-based role within Labcorp’s global operations center Salary: Competitive entry-level salary aligned with clinical research and CRO industry standards. Application Process Candidates interested in applying for the Data Management Associate I position can submit their applications through the official Labcorp careers portal. Apply Here: https://careers.labcorp.com/global/en/job/268086 Applicants are encouraged to apply early as entry-level roles within global clinical research organizations often receive a large number of applications. Frequently Asked Questions What does a Data Management Associate do in clinical research? A Data Management Associate supports the collection, validation, and management of research data generated during clinical or nonclinical studies. The role ensures that scientific data is organized, accurate, and ready for analysis and reporting. Who can apply for this Labcorp job? Candidates with bachelor’s degrees in life sciences, biotechnology, statistics, mathematics, computer science, or related disciplines can apply for this entry-level position. Is this job suitable for freshers? Yes. This is an entry-level clinical data management role, making it suitable for fresh graduates interested in starting careers in clinical research data operations. Are programming skills required? Programming knowledge in SAS, R, or Python is not mandatory but can be beneficial for candidates interested in data analytics roles within the life sciences industry. Where is the job located? The role is located in Bangalore, India, at Labcorp’s Brigade Twin Towers facility. Job Summary Category Details Company Labcorp Vacancies Data Management Associate I Required Education BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Statistics, BSc Mathematics, BSc Computer Science, BSc Information Systems, BCA, BTech Biotechnology, BTech Computer Science Experience Entry Level / Freshers Eligible [...] Read more...

Accenture Fresher Pharmacovigilance Vacancies Bangalore

March 13, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Accenture Pharmacovigilance New Associate Hiring – Bengaluru Accenture hiring Pharmacovigilance New Associates in Bengaluru. BAMS, BSc Nursing, Life Sciences. Fresher roles. Apply online. Accenture has opened hiring for the role of Pharmacovigilance Services New Associate at its Bengaluru location. This opportunity is ideal for freshers and early-career professionals from life sciences and healthcare backgrounds who are looking to build a long-term career in pharmacovigilance, drug safety, and regulatory compliance. With structured training, global exposure, and standardized safety operations, this role offers a strong entry point into the global drug safety ecosystem. Pharmacovigilance continues to be a high-demand domain due to increasing regulatory scrutiny, post-marketing surveillance requirements, and global clinical development activities. Joining Accenture in a drug safety role places candidates at the intersection of healthcare, data, and regulatory science, contributing directly to patient safety and public health outcomes. Company Overview Accenture is a global professional services organization with deep expertise across digital, cloud, security, and life sciences operations. Operating in more than 120 countries with a workforce of over 790,000 professionals, Accenture supports leading pharmaceutical, biotechnology, and healthcare organizations through technology-enabled services and intelligent operations. In the life sciences domain, Accenture plays a critical role in pharmacovigilance operations, clinical safety, regulatory compliance, and real-world evidence management. The company partners with global pharma clients to ensure timely adverse event reporting, regulatory submissions, and compliance with international safety regulations. Accenture’s strong governance framework, training programs, and global delivery model make it a trusted employer for careers in drug safety and pharmacovigilance. Job Role & Responsibilities As a Pharmacovigilance Services New Associate, you will support end-to-end drug safety operations and contribute to accurate and timely processing of adverse event data in global safety databases. Core Responsibilities Perform intake, triage, and case creation of Individual Case Safety Reports (ICSRs) Identify and process adverse events (AEs), serious adverse events (SAEs), and SUSARs Create and maintain cases in the global safety database as per client SOPs Perform case data entry, quality checks, and follow-up processing Ensure compliance with global regulatory timelines and submission requirements Conduct medical and drug coding using MedDRA and WHO-Drug dictionaries Draft case narratives and reviewer comments as per regulatory standards Perform duplicate checks, case corrections, and case deletions when required Support submission of safety reports through E2B and regulatory gateways Monitor and reconcile client mailboxes and intake sources Additional Responsibilities Assist in audits, inspections, and compliance activities Support pharmacovigilance projects and transition activities Perform document archiving and data validation activities Coordinate with cross-functional and client teams for safety deliverables Translate source documents and narratives when required Eligibility / Qualifications Required Educational Background Candidates must hold one of the following qualifications: Bachelor of Ayurvedic Medicine and Surgery (BAMS), BSc Nursing, Bachelor Degree in Life Sciences Experience Requirement 0 to 1 year of experience in pharmacovigilance or drug safety operations Freshers with strong subject knowledge are eligible Skill Requirements Knowledge of pharmacovigilance and drug safety concepts Understanding of adverse event reporting and case processing Familiarity with medical terminology Exposure to MedDRA and WHO-Drug dictionaries is preferred Basic knowledge of global safety databases is an advantage Proficiency in MS Office applications Strong medical writing and documentation skills Excellent English communication skills (reading, writing, listening, speaking) Location & Salary Job Location Bengaluru, Karnataka Salary Information Salary details are not disclosed and will be offered based on company norms, qualification, and interview performance. Pharmacovigilance roles fall under high-value healthcare analytics and compliance segments due to regulatory responsibility and global demand. Application Process Interested and eligible candidates must apply online through Accenture’s official career portal. Apply Here: https://www.accenture.com/in-en/careers/jobdetails?id=AIOC-S01621688_en&title=Pharmacovigilance+Services+New+Associate Frequently Asked Questions (FAQs) Who can apply for this Accenture pharmacovigilance role? Candidates with BAMS, BSc Nursing, or a bachelor’s degree in Life Sciences are eligible. Is this role suitable for freshers? Yes. Candidates with 0 to 1 year of experience can apply. What skills are required for pharmacovigilance jobs? Knowledge of adverse event reporting, medical terminology, MedDRA coding, and safety databases is preferred. Where is the job location? The position is based in Bengaluru, Karnataka. How can candidates apply? Applications must be submitted through Accenture’s official career portal. Category Details Company Accenture Vacancies Pharmacovigilance New Associate Required Education BAMS, BSc Nursing, Life Sciences Experience 0 to 1 Year [...] Read more...

Fortrea Hiring Fresher Pharmacovigilance – Safety Science Analyst

March 13, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Fortrea Hiring Safety Science Analyst – Pharmacovigilance Fresher Opportunity in Pune Fortrea is currently hiring for the position of Safety Science Analyst in Pune, India. This is a 6‑month contract role within the Clinical Safety / Pharmacovigilance department, designed primarily for healthcare and life sciences graduates who want to begin their careers in drug safety and pharmacovigilance operations. The opportunity is open to candidates with 0–1 year of safety experience, making it suitable for freshers and early‑career professionals interested in clinical safety, adverse event reporting, and global pharmacovigilance processes. The Safety Science Analyst will assist in handling safety data collected from clinical trials and post‑marketing surveillance programs, ensuring accurate processing of adverse events and compliance with regulatory reporting timelines. This role provides exposure to global safety databases, regulatory guidelines, and the end‑to‑end pharmacovigilance workflow used in modern pharmaceutical development. Professionals selected for this role will collaborate with global clinical safety teams, regulatory specialists, and pharmacovigilance experts to ensure patient safety information is processed accurately and efficiently. For candidates aiming to build careers in drug safety, clinical research, pharmacovigilance operations, and regulatory compliance, this role provides an excellent entry point into the pharmaceutical industry. Company Overview Fortrea is a global contract research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies throughout the clinical development lifecycle. The organization specializes in clinical trial management, pharmacovigilance, regulatory support, and data science services that help bring new medicines and therapies to patients faster. With decades of experience in clinical development, Fortrea partners with healthcare companies worldwide to manage clinical trials, monitor drug safety, and ensure compliance with international regulatory standards. The company operates across multiple therapeutic areas including oncology, cardiovascular diseases, neurology, immunology, and rare diseases. Fortrea’s pharmacovigilance and safety science teams play a critical role in monitoring adverse events, analyzing safety signals, and ensuring medicines meet global regulatory safety requirements. Through its global network of safety experts and clinical researchers, the organization contributes to improving patient outcomes and ensuring the safe use of medicines across international markets. Employees working at Fortrea gain exposure to advanced safety reporting systems, global clinical trial environments, and regulatory frameworks used by leading pharmaceutical companies worldwide. Job Role & Responsibilities The Safety Science Analyst supports pharmacovigilance and clinical safety operations by assisting with the collection, processing, and reporting of safety data related to pharmaceutical products. Key responsibilities include: Performing intake and triage of incoming safety reports from clinical trials and spontaneous reporting systems Processing adverse event reports according to regulatory guidelines and company procedures Entering safety data into adverse event tracking systems and pharmacovigilance databases Preparing patient narratives that summarize safety case information Coding adverse events using the MedDRA dictionary where applicable Supporting assessment of listedness against product labeling for marketed products Generating queries to obtain missing or inconsistent safety information Coordinating with medical reviewers and pharmacovigilance staff to resolve case queries Submitting expedited serious adverse event (SAE) reports to clients, investigators, and regulatory authorities Supporting submission of periodic safety reports and regulatory documentation Assisting with reconciliation of clinical safety databases Maintaining documentation related to global adverse event reporting requirements Supporting archival and documentation management for safety case files Ensuring compliance with internal quality systems, including SOPs and work instructions Collaborating with cross‑functional teams within pharmacovigilance and clinical safety departments This role ensures that adverse event data is captured accurately and reported within regulatory timelines, helping protect patient safety and maintain compliance with global drug safety regulations. Eligibility / Qualifications Candidates applying for this pharmacovigilance and clinical safety role should meet the following requirements. Required Education Candidates must hold a healthcare or life sciences degree. Relevant courses include: B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, Nursing, Pharmacology, Clinical Research, Life Sciences Experience 0–1 year of experience in pharmacovigilance or drug safety operations Freshers with healthcare or pharmacy backgrounds are eligible to apply Required Skills Strong attention to detail when handling clinical safety data Good written and verbal communication skills Ability to manage multiple safety cases and deadlines Knowledge of pharmacovigilance processes and adverse event reporting Familiarity with Microsoft Office tools and data entry systems Ability to work collaboratively in clinical safety teams Preferred Knowledge Basic understanding of MedDRA coding and pharmacovigilance terminology Awareness of regulatory safety reporting guidelines Location & Salary Job Location: Pune, Maharashtra, India Work Model: Office based role This position is offered as a 6‑month contract opportunity within Fortrea’s clinical safety operations team. Salary details for this position have not been publicly disclosed. Compensation typically depends on company policy and the candidate’s educational background or prior safety experience. Application Process Candidates interested in this pharmacovigilance job opportunity can apply through the official Fortrea careers portal. Apply here: https://careers.fortrea.com/us/en/job/261157/Safety-Science-Analyst-6-months-contract-Bengaluru-HCP-only Applicants are advised to submit their applications through the official website to ensure authenticity and avoid recruitment scams. Frequently Asked Questions What does a Safety Science Analyst do? A Safety Science Analyst processes adverse event reports, enters safety data into pharmacovigilance systems, prepares patient narratives, and supports regulatory reporting for clinical trials and marketed medicines. Who can apply for this role? Candidates with healthcare or pharmacy degrees such as B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, or Nursing can apply. Is this role suitable for freshers? Yes. Candidates with 0–1 year of safety or pharmacovigilance experience can apply for this role. What systems are commonly used in pharmacovigilance roles? Pharmacovigilance professionals typically work with safety databases, adverse event reporting systems, and coding dictionaries such as MedDRA. How can I apply for this job? Candidates can apply through the official Fortrea careers website using the application link provided above. Job Summary Company Fortrea Vacancies Safety Science Analyst Required Education B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, Nursing, Pharmacology, Clinical Research, Life Sciences Experience 0–1 year pharmacovigilance or safety experience [...] Read more...

ICON Plc Pharmacovigilance Entry Level Vacancies: Pharmacovigilance Assistant I

March 13, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Are you looking to kick-start your career in pharmacovigilance? ICON Plc is offering entry-level vacancies for Pharmacovigilance Assistants in Chennai. Join our team at the Drug Safety ICON Full Service & Corporate Support Office and be a part of our mission to advance and improve patients’ lives. About ICON ICON is driven by a culture of accountability, collaboration, partnership, and integrity. We aim to be the Clinical Research Organisation that delivers excellence to our clients and patients at every touch-point. If you share our vision and are passionate about making a difference in healthcare, we invite you to join us. Pharmacovigilance Assistant I Job Responsibilities As a Pharmacovigilance Assistant at ICON Plc, your responsibilities will include: Business Support: Receives and distributes incoming safety notifications (such as exception approvals, hospital records, SAEs, SAE Hotline calls and other safety events via eFax, e-mail and safety mailboxes) to the appropriate project teams or to Sponsor contacts as per assignment; or surveillance of Safety Reporting specific mailboxes. Initiates appropriate actions to protect data privacy with regards to received unrequested personal identifiers. Maintains data entry for SAEs and miscellaneous tracking logs for all current projects. Prepares and submits courier shipments and electronic safety submissions on behalf of the project teams, including acknowledgement uploads to Safety Reporting System and maintenance of address data for safety submissions. Case tracker management and support Distribution of safety related documents like Clinical Trial Application (CTA), Power of Attorney (PoA) or delegation documents, and website searches as support to the safety reporting intelligence team. Uploads documents into the electronic Trial Master File (eTMF) and tracks the status in the Safety Tracking Tools. Downloads Safety Reporting Post-Marketing ICSR. Completes EudraVigilance acknowledgement of receipt (AoR) tracking in Safety Reporting System. Safety Reporting (CA Country Portal submissions, Monitoring of mailboxes and/or Client Portal, Support for expedited and periodic reporting and Bulk report submission and reconciliation) Performs the Translation Management Process as assigned. Perform regular testing of SAE Hotline, departmental phone lines, fax numbers and email addresses (general and project specific) as required; documents results. Maintain departmental and global calendars as required. Completion of monthly metrics. Perform offsite archiving activities as required. Applies knowledge and adheres to company policies and procedures including corporate guidelines and best practices. Flag errors/non-conformance to established processes. Applies knowledge of computerized information systems and standard application software (Windows, MS Office). Identifies and recognizes problems that have established precedents and limited impact. Refers non-standard questions and problems to higher levels. Project Management Support: Organizes project team and client meetings including scheduling, agendas, preparation of presentations and meeting minutes. Organizes, reviews and manages project specific information and material following applicable company processes, (such as organizational charts, Project Management Plans, project status reports). Supports the Project Manager with financial tasks. Support and processes purchase orders and project invoices. Acts as gatekeepers for eTMF and project file and maintains project specific email distribution lists. Uploads and files all documents within allotted timeframe into the electronic Trial Master File (eTMF) or Trial Master File (TMF), including package preparation, reconciliation of the TMF and the safety tracking tools for inspection readiness, sampling and coherence QC and query resolution and follow up. Monitoring and filing of project specific mailboxes. Maintains a training matrix, including assigning and tracking project-specific training and tracking training compliance as applicable in the relevant system(s). Maintenance, coordination and access of project Enterprise Document and Content Management Systems (EDCMS) and mapped drives etc. Monitors project team’s approved Curriculum Vitae (CV) dates in eTMF or Project File for compliance with applicable SOP. Updates project metrics and team members in applicable systems. Perform other activities as identified and requested by management. Benefits of Working at ICON We offer competitive salary packages, annual bonuses, health-related benefits, retirement plans, and a supportive environment that encourages talent and high performance. ICON is an equal opportunity and inclusive employer committed to providing a workplace free of discrimination and harassment. Join us at ICON Plc in Chennai and embark on a rewarding career journey in pharmacovigilance. Apply now to be part of our dynamic team and contribute to shaping the future of drug safety. Apply Online [...] Read more...

SIRO Medical Writing Hiring Regulatory Medical Writer

March 11, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now SIRO Medical Writing Regulatory Writer Jobs India Life Sciences, Pharmacy professionals with 5+ yrs experience can apply for Regulatory Medical Writer role at SIRO Medical Writing Pvt Ltd. SIRO Medical Writing Pvt. Ltd. has announced an exciting opportunity for experienced professionals in the Regulatory Medical Writing domain. The organization is currently hiring skilled candidates for the position of Regulatory Medical Writer, offering professionals the chance to contribute to global pharmaceutical and clinical research documentation. Medical writing plays a critical role in the pharmaceutical and clinical research industry. Regulatory medical writers are responsible for preparing complex scientific and regulatory documents that support drug development, clinical trials, and regulatory approvals. These documents ensure that pharmaceutical products meet strict global standards before reaching patients. SIRO Medical Writing Pvt. Ltd. is looking for professionals with 5+ years of experience in regulatory medical writing, particularly in drafting and reviewing regulatory documents such as Clinical Study Reports (CSRs), Protocols, Investigator Brochures (IBs), Informed Consent Documents (ICDs), narratives, tables of studies, and eCTD summaries. Professionals working in regulatory medical writing play an important role in supporting global pharmaceutical companies by preparing accurate, compliant, and scientifically sound documentation required by regulatory authorities such as USFDA, EMA, MHRA, and other global health agencies. For professionals seeking to advance their careers in clinical research documentation, regulatory submissions, and pharmaceutical regulatory writing, this role provides an opportunity to work in a highly specialized and globally recognized domain. Company Overview SIRO Medical Writing Pvt. Ltd. is part of the SIRO Clinpharm group, a well‑known clinical research organization (CRO) that provides integrated clinical research and regulatory services to global pharmaceutical, biotechnology, and medical device companies. The organization specializes in providing high‑quality regulatory documentation and scientific writing support throughout the drug development lifecycle. SIRO supports pharmaceutical sponsors by developing regulatory documents required for clinical trial submissions, regulatory approvals, and marketing authorization applications. The company’s services include: • Regulatory medical writing • Clinical study report preparation • Clinical protocol development • Regulatory submission documentation • eCTD and dossier support • Clinical research documentation review SIRO Medical Writing teams work closely with clinical research professionals, regulatory affairs specialists, biostatisticians, and pharmaceutical scientists to ensure that documentation submitted to regulatory agencies meets strict scientific and compliance standards. By maintaining adherence to international regulatory guidelines such as ICH guidelines, GCP standards, and global regulatory submission frameworks, SIRO ensures that documentation produced by its teams supports the safe and effective development of pharmaceutical products. Professionals working at SIRO gain exposure to global pharmaceutical projects and advanced regulatory documentation systems used in international clinical trials. Job Role & Responsibilities The Regulatory Medical Writer role focuses on preparing and reviewing scientific and regulatory documents required for pharmaceutical clinical development and regulatory submissions. Regulatory Document Preparation Medical writers are responsible for developing regulatory documents used in clinical trials and regulatory submissions. Key responsibilities include: • Drafting Clinical Study Reports (CSRs) • Preparing clinical trial protocols • Writing Investigator Brochures (IBs) • Developing Informed Consent Documents (ICDs) These documents are critical for ensuring transparency and compliance in clinical research activities. Regulatory Submission Support Medical writers assist regulatory teams in preparing documentation required for global regulatory submissions. Key responsibilities include: • Preparing tables of studies and clinical summaries • Supporting eCTD submission documentation • Drafting regulatory summaries and reports • Ensuring documentation meets regulatory submission standards These activities ensure that regulatory agencies receive well‑structured scientific data supporting pharmaceutical product approvals. Scientific Review and Quality Checks Regulatory medical writers are responsible for reviewing documentation to ensure scientific accuracy and regulatory compliance. Key responsibilities include: • Reviewing clinical documents for consistency and accuracy • Verifying data presented in study reports • Ensuring compliance with regulatory guidelines • Maintaining document version control and documentation integrity These review activities help maintain the reliability and credibility of clinical research documentation. Collaboration with Cross‑Functional Teams Medical writing teams collaborate with several departments during document preparation. Key responsibilities include: • Coordinating with clinical research teams • Working with biostatistics and data management teams • Supporting regulatory affairs teams during submission preparation • Addressing document review comments and revisions Effective collaboration ensures that regulatory documentation accurately reflects clinical research findings. Eligibility / Qualifications SIRO Medical Writing Pvt. Ltd. is seeking experienced professionals with academic backgrounds in life sciences and pharmaceutical sciences. Required Educational Qualifications Relevant qualifications include: B.Pharm, M.Pharm, Pharm.D, M.Sc Life Sciences Relevant academic disciplines include: Pharmacy, Pharmacology, Clinical Research, Biotechnology, Microbiology, Biochemistry, Life Sciences These educational backgrounds provide foundational knowledge in clinical research methodologies, pharmaceutical sciences, drug development processes, and regulatory documentation standards. Experience Requirement Candidates must have minimum 5+ years of experience in regulatory medical writing. Relevant experience includes: • Clinical study report writing • Regulatory documentation drafting • Clinical protocol preparation • Regulatory submission documentation • eCTD summary preparation Professionals with experience working in clinical research organizations (CROs) or pharmaceutical regulatory documentation teams will be preferred. Required Skills Ideal candidates should possess: • Strong scientific writing skills • Understanding of clinical research documentation • Knowledge of regulatory guidelines • Ability to analyze clinical data • Excellent attention to detail and documentation accuracy Experience working with clinical research documentation systems and regulatory submission platforms will be an advantage. Location & Salary Job Location SIRO Medical Writing Pvt. Ltd. India (office location based on company assignment) Medical writing professionals often work in major pharmaceutical hubs where clinical research and regulatory documentation teams collaborate with global pharmaceutical sponsors. Salary Salary packages are determined based on candidate experience, expertise, and company policies. Regulatory medical writing professionals typically receive competitive compensation packages due to the specialized nature of their work. Application Process Interested candidates who meet the eligibility criteria can apply by sending their updated resumes. Send your CV to: vedanshi.hemani@siroclinpharm.com Applicants should include the following information when submitting their resume: • Full name • Educational qualifications • Total experience in medical writing • Experience in regulatory documentation • Notice period availability Shortlisted candidates will be contacted by the recruitment team for further discussions and interviews. Why Build a Career in Regulatory Medical Writing Regulatory medical writing is a highly specialized profession within the pharmaceutical and clinical research industries. Medical writers translate complex clinical and scientific data into structured regulatory documents used for drug development and regulatory approvals. Professionals working in this field gain expertise in: • Clinical research documentation • Pharmaceutical regulatory guidelines • Drug development processes • Regulatory submission systems • Scientific and regulatory writing techniques Medical writing professionals play a vital role in the pharmaceutical industry by ensuring that regulatory authorities receive clear, accurate, and compliant documentation. Career opportunities in regulatory medical writing include: • Senior Medical Writer • Regulatory Documentation Manager • Clinical Research Documentation Specialist • Regulatory Affairs Medical Writer As pharmaceutical research continues to expand globally, the demand for experienced medical writers continues to grow across pharmaceutical companies, CROs, and biotechnology organizations. Frequently Asked Questions (FAQs) Who can apply for the SIRO Medical Writer role? Professionals with life sciences or pharmacy qualifications and at least 5 years of regulatory medical writing experience can apply. What documents should candidates have experience with? Candidates should have experience drafting Clinical Study Reports, protocols, Investigator Brochures, Informed Consent Documents, and eCTD summaries. What industry does this role belong to? The role belongs to the pharmaceutical and clinical research industry. How can candidates apply? Candidates can send their updated resume to the official HR email mentioned in the job posting. What skills are important for medical writing? Strong scientific writing, understanding of regulatory guidelines, and experience with clinical documentation are essential skills. Job Summary Company SIRO Medical Writing Pvt Ltd Vacancies Regulatory Medical Writer Required Education B.Pharm, M.Pharm, Pharm.D, M.Sc Life Sciences Experience 5+ Years [...] Read more...

Genuine Hiring Production / Manufacturing Trainee

March 11, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Genuine Biosystem BSc MSc Trainee Jobs | Tamil Nadu BSc, MSc Life Sciences fresher vacancies at Genuine Biosystem Pvt Ltd Oragadam for Production Trainee in IVD manufacturing. Genuine Biosystem Pvt Ltd has announced fresh career opportunities for Life Sciences graduates interested in building their careers in the In-Vitro Diagnostics (IVD) manufacturing industry. The company is currently hiring Production / Manufacturing Trainees for its facility located in Oragadam, Tamil Nadu. This opportunity is ideal for B.Sc and M.Sc Life Sciences freshers who want to begin their professional journey in the biotechnology and diagnostic manufacturing sector. The global healthcare industry depends heavily on diagnostic technologies to detect diseases, monitor treatment responses, and support preventive healthcare strategies. In-Vitro Diagnostics (IVD) manufacturing companies produce diagnostic kits, reagents, and laboratory testing products that enable hospitals, laboratories, and healthcare providers to deliver accurate medical testing results. Production trainees working in the IVD manufacturing sector play an essential role in maintaining product quality, ensuring accurate formulation of diagnostic reagents, and following strict manufacturing and regulatory guidelines such as Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs). Genuine Biosystem Pvt Ltd is seeking motivated candidates with academic backgrounds in Biotechnology, Microbiology, Biochemistry, Biology, and other Life Science disciplines who are eager to gain hands-on experience in biotechnology manufacturing processes, diagnostic reagent production, quality documentation systems, and laboratory handling procedures. For fresh graduates looking to establish a strong foundation in the biotechnology and healthcare diagnostics industry, this opportunity offers practical exposure to modern manufacturing environments and regulated production systems. Company Overview Genuine Biosystem Pvt Ltd is a biotechnology company focused on the manufacturing of In-Vitro Diagnostic (IVD) products used in clinical laboratories, hospitals, and research institutions. The organization is committed to providing reliable diagnostic solutions that help healthcare professionals detect diseases and monitor patient health conditions accurately. The IVD sector is a critical part of the global healthcare ecosystem. Diagnostic kits and laboratory reagents produced by companies like Genuine Biosystem support medical professionals in identifying infections, chronic diseases, genetic conditions, and metabolic disorders. The company operates manufacturing processes that comply with strict regulatory guidelines and quality systems required for diagnostic product manufacturing. These processes include: • Diagnostic reagent formulation • Quality-controlled production environments • Standardized batch manufacturing procedures • Regulatory documentation and product traceability By maintaining adherence to GMP standards and quality management systems, Genuine Biosystem ensures the safety, accuracy, and reliability of its diagnostic products. The company’s manufacturing facility located in Oragadam, Tamil Nadu is strategically positioned within a growing biotechnology and pharmaceutical manufacturing cluster. Employees working at this facility gain exposure to biotechnology production technologies, laboratory process management, diagnostic product development, and regulated manufacturing operations. Professionals joining the organization will develop technical skills that are highly valuable across biotechnology companies, diagnostic laboratories, pharmaceutical manufacturers, and research institutions. Job Role & Responsibilities The Production / Manufacturing Trainee role focuses on supporting the manufacturing processes involved in producing diagnostic reagents and laboratory testing kits. Diagnostic Reagent Manufacturing Support Production trainees assist senior manufacturing staff in preparing diagnostic reagents used in laboratory testing kits. Key responsibilities include: • Assisting in preparation and production of diagnostic reagents • Supporting batch manufacturing activities according to approved procedures • Maintaining cleanliness and contamination control during manufacturing processes • Following established SOPs and GMP guidelines These activities ensure the consistent production of reliable diagnostic products. Filling, Labeling, and Packaging Operations IVD manufacturing requires careful handling and packaging of diagnostic kits to maintain product integrity. Key responsibilities include: • Performing filling operations for diagnostic reagents • Supporting labeling and packaging of finished IVD products • Verifying product labeling information and batch details • Maintaining proper product identification and traceability Packaging operations ensure that diagnostic products reach healthcare facilities safely and accurately labeled. Production Documentation and Batch Records Accurate documentation is a critical requirement in regulated manufacturing environments. Key responsibilities include: • Recording production activities in batch manufacturing records • Maintaining documentation according to GMP requirements • Reporting production details to supervisors • Ensuring traceability of raw materials and finished products These documentation practices help maintain regulatory compliance and product quality standards. Material Handling and Storage Proper handling of raw materials and finished goods ensures product safety and quality. Key responsibilities include: • Ensuring correct storage conditions for raw materials • Maintaining inventory of manufacturing materials • Handling materials according to safety guidelines • Supporting stock verification activities Effective material management prevents contamination and ensures efficient manufacturing operations. Eligibility / Qualifications Genuine Biosystem Pvt Ltd is inviting applications from fresh graduates with life sciences academic backgrounds. Required Educational Qualifications B.Sc Life Sciences, M.Sc Life Sciences Relevant academic disciplines include: Biotechnology, Microbiology, Biochemistry, Biology, Biomedical Science, Life Sciences These programs provide foundational knowledge in biological systems, laboratory techniques, microbiology methods, and biotechnology manufacturing concepts. Experience Requirement Freshers are eligible to apply. Candidates who recently completed their academic programs and are interested in biotechnology manufacturing careers are encouraged to apply. Required Skills Ideal candidates should demonstrate: • Basic knowledge of laboratory practices • Understanding of biotechnology or microbiology principles • Attention to detail and documentation accuracy • Ability to follow SOPs and safety procedures • Willingness to work in manufacturing environments Candidates with exposure to laboratory research, biotechnology experiments, or diagnostic testing procedures will have an advantage. Location & Salary Job Location Genuine Biosystem Pvt Ltd Oragadam, Tamil Nadu Oragadam is an emerging industrial and biotechnology manufacturing hub in Tamil Nadu, hosting several pharmaceutical and biotechnology companies. Salary Salary for the Production / Manufacturing Trainee position will be determined according to company policies, candidate qualifications, and industry standards. Entry-level biotechnology manufacturing roles typically include training programs and opportunities for career development. Application Process Interested candidates can apply by submitting their updated resumes to the company’s HR department. Send your CV to: admin-hr@genuinebiosystem.com For inquiries, candidates may contact: +91 63830 66400 Applicants should include the following information when submitting their resume: • Full name • Educational qualification • Contact details • Internship or project experience (if available) Shortlisted candidates will be contacted by the recruitment team for further interview rounds. Why Start Your Career in the IVD Manufacturing Industry The In-Vitro Diagnostics (IVD) industry is one of the fastest growing segments within the healthcare and biotechnology sector. Diagnostic testing plays a crucial role in disease detection, treatment monitoring, and public health surveillance. Professionals working in diagnostic manufacturing gain valuable experience in: • Biotechnology production processes • Laboratory reagent formulation • GMP-compliant manufacturing systems • Diagnostic kit packaging and labeling • Quality documentation and traceability These skills open career opportunities across several industries including: • Biotechnology companies • Pharmaceutical manufacturing • Diagnostic laboratories • Medical device companies • Research and development organizations As healthcare systems continue to expand globally, the demand for reliable diagnostic testing products and trained biotechnology professionals continues to grow. Frequently Asked Questions (FAQs) Who can apply for the Genuine Biosystem trainee role? Fresh graduates with B.Sc or M.Sc degrees in Life Sciences disciplines such as Biotechnology, Microbiology, and Biochemistry can apply. Is prior experience required? No. This position is designed specifically for fresh graduates starting their careers in biotechnology manufacturing. What industry does the company operate in? Genuine Biosystem Pvt Ltd operates in the In-Vitro Diagnostics (IVD) manufacturing industry. Where is the job location? The job is based at the company’s manufacturing facility in Oragadam, Tamil Nadu. How can candidates apply? Candidates can submit their resume to the official HR email address provided in the job posting. Job Summary Company Genuine Biosystem Pvt Ltd Vacancies Production / Manufacturing Trainee Required Education B.Sc Life Sciences, M.Sc Life Sciences Experience Freshers [...] Read more...

Axis walk‑in Bioanalytical & Medical Writing

MSc, B Pharm, M Pharm Fresher Hiring as Associate STEM Content Analyst Chemistry | Clarivate

March 11, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Clarivate Hiring Associate STEM Content Analyst in Hyderabad – B.Pharm, M.Pharm & MSc Freshers Eligible Clarivate has announced a hiring opportunity for the role of Associate STEM Content Analyst within its Clinical Studies team located in Hyderabad, Telangana. The position is offered in a hybrid work model and is open to freshers or candidates with up to six months of experience in clinical research analysis or scientific data review. This role sits within the Life Sciences and Healthcare division and supports Clarivate’s globally recognized intelligence platforms such as Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. These platforms are widely used by pharmaceutical companies, biotechnology firms, and research organizations to track drug pipelines, analyze clinical trials, and support strategic decisions in drug development. For graduates in pharmacy and life sciences, this opening provides a valuable entry point into the growing field of clinical research intelligence, pharmaceutical data analysis, and drug development research support. Professionals joining this team will contribute to maintaining accurate clinical trial databases used by global pharmaceutical innovators. Company Overview Clarivate is a global analytics and insights company that provides trusted data, research tools, and technology solutions to organizations across life sciences, healthcare, academia, and intellectual property sectors. The company is best known for its powerful information platforms that help researchers, pharmaceutical companies, and academic institutions make evidence-based decisions. Clarivate products support activities such as drug discovery, clinical research, regulatory planning, and scientific publishing. Within the life sciences industry, Clarivate plays a major role in delivering drug pipeline intelligence, clinical trial analytics, and scientific research insights. Pharmaceutical companies rely on Clarivate’s data platforms to track emerging therapies, analyze competitive landscapes, and evaluate clinical development strategies. The Hyderabad office supports several global research and analytics operations, particularly in life sciences data management and clinical intelligence services. Professionals working in these teams contribute directly to improving the availability and accuracy of pharmaceutical research data used worldwide. By joining Clarivate, candidates gain exposure to global clinical trial information, drug discovery programs, and pharmaceutical innovation trends while working in a collaborative and knowledge-driven environment. Job Role & Responsibilities The Associate STEM Content Analyst will work as part of the Clinical Studies team responsible for maintaining and updating clinical trial intelligence databases used by global pharmaceutical organizations. The role involves reviewing scientific information from various sources, analyzing clinical trial data, and ensuring accurate records within Clarivate’s research platforms. Key responsibilities include: Monitoring multiple scientific and clinical information sources such as conferences, trial registries, press releases, and research publications Collecting, reviewing, and validating clinical trial information related to pharmaceutical drug development Updating clinical study records within the Cortellis intelligence databases Cross-referencing information from multiple sources to ensure accuracy and completeness of clinical trial data Maintaining up-to-date records of drug development programs and clinical study progress Interpreting complex clinical trial information and converting it into structured database entries Meeting weekly productivity and data quality targets set by the clinical research team Ensuring data quality and compliance with internal editorial standards Identifying discrepancies in clinical trial information and resolving them through research and analysis This role requires strong attention to detail and analytical thinking, as the accuracy of the clinical database directly impacts research decisions made by pharmaceutical companies. Eligibility / Qualifications Candidates applying for the Associate STEM Content Analyst role should have a strong academic background in life sciences or pharmaceutical sciences and a genuine interest in clinical research and drug development. Educational Qualification Candidates should possess one of the following degrees from a recognized university: B.Pharm, M.Pharm, MSc Biotechnology, MSc Microbiology, MSc Life Sciences, MSc Biochemistry. These academic programs provide foundational knowledge in pharmacology, drug development, microbiology, biotechnology, and clinical research processes that are essential for analyzing clinical study data. Experience The position is suitable for freshers or candidates with up to six months of relevant experience in clinical research analysis, scientific content review, or pharmaceutical data research. Experience in secondary research related to clinical trials or pharmaceutical information will be considered an advantage but is not mandatory. Required Skills Candidates should demonstrate the following competencies: Strong understanding of clinical trials, drug pipelines, and pharmaceutical development phases Ability to interpret complex clinical study data and research information Excellent written and verbal communication skills in English Strong analytical and problem-solving abilities Ability to conduct research across multiple scientific information sources Attention to detail when reviewing and updating clinical research data Ability to work within defined productivity targets and quality standards Candidates who are curious, research-oriented, and comfortable working with large volumes of scientific information are likely to perform well in this role. Location & Salary Location: Hyderabad, Telangana, India Work Model: Hybrid (Monday to Friday) Working Hours: 9:00 AM – 6:00 PM Application Process Interested candidates can apply through the official Clarivate careers portal using the link below: Apply Online: https://careers.clarivate.com/job/CLACLAGBJREQ134953EXTERNALENGB/Associate-STEM-Content-Analyst Applicants may be contacted by the Clarivate recruitment team for further evaluation, which may include assessments of analytical skills, understanding of clinical research concepts, and communication ability. Candidates are advised to keep their updated resumes ready and highlight any coursework or project experience related to clinical trials, drug development, or pharmaceutical research. Frequently Asked Questions (FAQs) Who can apply for the Clarivate Associate STEM Content Analyst role? Candidates with B.Pharm, M.Pharm, or MSc degrees in Biotechnology, Microbiology, Life Sciences, or Biochemistry can apply for this role. Are freshers eligible for this position? Yes. Fresh graduates or candidates with up to six months of experience in clinical research analysis or scientific research support are eligible. What does a STEM Content Analyst do in the pharmaceutical industry? They collect, analyze, and maintain clinical trial data, drug pipeline information, and scientific research updates used by pharmaceutical companies for strategic decision-making. Where is the job located? The role is based in Hyderabad, Telangana, with a hybrid working model. What career growth opportunities exist in clinical intelligence roles? Professionals can grow into roles such as Clinical Research Analyst, Drug Pipeline Intelligence Specialist, Medical Information Analyst, or Life Sciences Research Consultant. Summary Company Clarivate Vacancies Associate STEM Content Analyst Required Education B.Pharm, M.Pharm, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Life Sciences Experience Freshers or Up to 6 Months Experience in Clinical Research / Data Analysis [...] Read more...

Reliance Retail Hiring Pharmacists in Bengaluru – D.Pharm & B.Pharm Candidates Eligible

March 10, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Reliance Retail has announced new hiring for the position of Pharmacist in the Operations Department at its pharmacy outlets in Bengaluru, Karnataka. The full-time on-site opportunity is open to qualified pharmacy professionals with D.Pharm or B.Pharm qualifications and a valid Karnataka pharmacist license. The recruitment highlights growing demand for licensed pharmacists in organized retail pharmacy chains across India. As healthcare access expands through modern pharmacy networks, pharmacists play a critical role in medication dispensing, patient counseling, inventory control, and regulatory compliance. For pharmacy graduates seeking stable careers in retail pharmacy operations and patient care services, Reliance Retail’s pharmacy network offers exposure to high-volume healthcare environments and structured pharmacy management systems. Company Overview Reliance Retail is one of India’s largest retail companies and part of the Reliance Industries Group. The organization operates thousands of stores across the country spanning grocery, electronics, fashion, digital services, and healthcare retail. Within healthcare, Reliance Retail operates pharmacy outlets that provide prescription medicines, over-the-counter healthcare products, wellness items, and essential medical supplies. The company focuses on delivering affordable medicines and reliable healthcare services to millions of customers across urban and semi-urban regions. The pharmacy division emphasizes regulatory compliance, patient safety, and responsible medication dispensing practices. Pharmacists working within the network collaborate with healthcare professionals and customers to ensure accurate medication usage and improved patient outcomes. Reliance Retail also provides structured operational systems, digital billing platforms, and inventory management technologies that support efficient pharmacy store management. Job Role & Responsibilities The Pharmacist will be responsible for ensuring safe medication dispensing and delivering professional pharmaceutical care to customers visiting the pharmacy outlet. Key responsibilities include: Dispensing prescription medicines and over-the-counter pharmaceutical products accurately Reviewing prescriptions to verify correctness and prevent dispensing errors Providing guidance to customers regarding dosage instructions, medication usage, storage, and potential side effects Maintaining accurate records of prescriptions and pharmacy inventory as per regulatory requirements Ensuring full compliance with pharmacy regulations, drug safety standards, and store policies Conducting routine stock verification and maintaining optimal medicine inventory levels Coordinating ordering and replenishment of pharmaceutical products when stock levels decrease Handling billing transactions and maintaining documentation for pharmacy operations Supporting insurance documentation and prescription record management when required Collaborating with doctors, healthcare professionals, and suppliers when necessary Maintaining hygiene, cleanliness, and organization inside the pharmacy outlet Delivering high-quality customer service while addressing patient queries professionally Pharmacists in organized retail environments play a crucial role in ensuring the correct use of medications and improving public health awareness. Eligibility / Qualifications Candidates interested in this pharmacist position should possess strong pharmaceutical knowledge, attention to detail, and excellent communication skills to guide patients effectively. Educational Qualification Candidates must hold a recognized pharmacy qualification such as: Diploma in Pharmacy (D.Pharm), Bachelor of Pharmacy (B.Pharm) Mandatory Requirement Valid Karnataka State Pharmacy Council registration / pharmacist license Preferred Skills and Competencies Candidates should ideally demonstrate: Strong knowledge of pharmaceutical medicines and drug regulations Ability to interpret prescriptions accurately Excellent communication and patient counseling skills High level of accuracy and attention to detail Ability to work in fast-paced retail pharmacy environments Basic computer knowledge including pharmacy billing software and inventory systems Ethical conduct and professional responsibility in medication dispensing Preferred Experience Although not mandatory, candidates with prior experience in retail pharmacy or hospital pharmacy environments may have an advantage during the selection process. Knowledge of drug interactions, pharmacy management software, and inventory control systems is also beneficial. Location & Salary Location: Bengaluru, Karnataka, India Work Mode: On-site Application Process Interested candidates can apply through the official job listing using the link below: Apply Online: https://www.linkedin.com/jobs/view/4350160239/ Applicants may be contacted by the recruitment team for further evaluation, interview scheduling, and verification of pharmacist registration credentials. Candidates should ensure their professional documents and pharmacy license details are updated before applying. Frequently Asked Questions (FAQs) Who can apply for the Reliance Retail Pharmacist position? Candidates holding D.Pharm or B.Pharm qualifications with valid Karnataka pharmacist registration are eligible to apply for this role. Is prior experience required for this pharmacist role? Experience may be required depending on the store’s operational needs, but candidates with retail or hospital pharmacy experience are generally preferred. What are the key responsibilities of a retail pharmacist? Retail pharmacists dispense medications, review prescriptions, provide patient counseling, manage pharmacy inventory, maintain regulatory compliance, and ensure safe medication practices. Where is the job located? The position is located in Bengaluru, Karnataka, and requires on-site work within Reliance Retail pharmacy operations. What skills are important for pharmacist jobs? Key skills include medication knowledge, prescription interpretation, patient counseling, communication skills, pharmacy law compliance, and inventory management. Summary Company Reliance Retail Vacancies Pharmacist Required Education Diploma in Pharmacy (D.Pharm), Bachelor of Pharmacy (B.Pharm) Experience Retail Pharmacy / Hospital Pharmacy Experience Preferred [...] Read more...

Lupin Walk‑In Production, QA & QC

Emcure Walk‑In Production, QC & Packing

Virchow walk‑in Trainee Executive, Trainee Operator

Promea Hiring Production & Warehouse

March 10, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BSc BPharm Fresher Jobs | Promea Biologics Production Hyderabad BSc, MSc, BPharm fresher vacancies at Promea Therapeutics Sangareddy for Biologics, LVP Production & Warehouse roles. Promea Therapeutics Pvt. Ltd. is inviting applications for multiple positions across Biologics Production, LVP Manufacturing, Warehouse Operations, Administration, and Technical Operator roles at its advanced pharmaceutical manufacturing facility located in the Medical Devices Park, Sangareddy, Telangana. The company is hiring both fresh graduates and experienced professionals who want to develop long‑term careers in biopharmaceutical manufacturing, sterile production technology, and GMP‑regulated pharmaceutical environments. This recruitment drive is particularly attractive for fresh graduates from life sciences and pharmaceutical backgrounds who want practical exposure to biologics manufacturing, intravenous (IV) fluid production, Blow‑Fill‑Seal (BFS) technology, downstream bioprocessing, and pharmaceutical warehouse management systems. Promea Therapeutics is part of India’s rapidly expanding biotechnology and biopharmaceutical ecosystem. Professionals joining the company will gain hands‑on experience with GMP‑compliant biologics manufacturing processes, pharmaceutical production operations, sterile injectable manufacturing, and pharmaceutical quality systems. These roles are designed to help young professionals build expertise in biopharmaceutical manufacturing technology, regulated pharmaceutical production systems, and pharmaceutical supply chain operations, which are some of the most valuable skills in the global life sciences industry. Company Overview Promea Therapeutics Pvt. Ltd. is a biotechnology and pharmaceutical manufacturing company specializing in biologics development, plasma‑derived therapeutics, and advanced pharmaceutical manufacturing technologies. The company operates within India’s rapidly growing biopharmaceutical industry and focuses on delivering innovative therapies that support global healthcare needs. Biopharmaceutical companies play a critical role in modern healthcare by producing complex biological medicines such as plasma‑derived therapies, recombinant proteins, vaccines, and other advanced therapeutic products. Manufacturing these products requires sophisticated production technologies, sterile processing environments, and strict regulatory compliance systems. Promea’s facility located in Medical Devices Park, Sultanpur, Ameenpur, Sangareddy, Telangana is designed to support modern pharmaceutical and biotechnology manufacturing operations. The plant includes advanced equipment for sterile manufacturing, biologics processing, filtration technologies, purification systems, and pharmaceutical packaging operations. The company operates under internationally recognized pharmaceutical and biotechnology regulatory standards such as: • Current Good Manufacturing Practices (cGMP) • Good Documentation Practices (GDP) • Quality Management Systems (QMS) • Pharmaceutical regulatory compliance frameworks These standards ensure that pharmaceutical and biological products manufactured at the facility meet strict safety, quality, and regulatory requirements. By joining Promea Therapeutics, professionals gain exposure to biopharmaceutical production systems, sterile injectable manufacturing technology, pharmaceutical quality compliance systems, and global biotech manufacturing standards. Job Role & Responsibilities Promea Therapeutics is hiring across several operational departments that support pharmaceutical and biotechnology manufacturing. LVP Production – Junior Executive Large Volume Parenteral (LVP) production involves manufacturing sterile IV fluids used in hospitals and healthcare settings. Key responsibilities include: • Performing batch calculations and material dispensing • Supporting production batch preparation according to cGMP and GDP standards • Monitoring production operations during IV fluid manufacturing • Maintaining accurate production documentation and logbooks • Coordinating with Quality Assurance, Engineering, and Quality Control teams LVP production professionals ensure sterile pharmaceutical products are manufactured safely and consistently. Blow‑Fill‑Seal (BFS) Operator – LVP FFS BFS technology is widely used in pharmaceutical sterile manufacturing to produce injectable products without contamination. Key responsibilities include: • Operating Blow‑Fill‑Seal machines used in IV fluid production • Setting machine parameters such as temperature, pressure, and filling volume • Monitoring molding, filling, and sealing operations • Performing in‑process quality checks including leak tests and visual inspections • Ensuring compliance with GMP and sterile manufacturing guidelines Working with BFS technology provides valuable experience in advanced sterile pharmaceutical manufacturing systems. Biologics Production – Junior Executive Biologics manufacturing involves processing biological materials used in advanced therapeutic products. Key responsibilities include: • Supporting downstream bioprocessing operations • Preparing buffers and solutions used in biologics manufacturing • Handling laboratory instruments such as pH meters and spectrophotometers • Performing depth filtration processes • Supporting protein purification using technologies such as Tangential Flow Filtration (TFF) These activities are critical in producing high‑quality biologic medicines used in modern healthcare. Warehouse – Junior Executive Warehouse operations ensure proper handling and storage of pharmaceutical materials. Key responsibilities include: • Raw material and packaging material dispensing • Maintaining finished goods inventory records • Monitoring material movement across production departments • Ensuring compliance with GMP and pharmaceutical storage standards • Maintaining documentation for inventory and material reconciliation Pharmaceutical warehouse teams play a crucial role in maintaining supply chain efficiency. Administration – Supervisor Administrative supervisors ensure smooth operations of facility support services. Key responsibilities include: • Managing housekeeping and facility maintenance activities • Supervising contract workforce attendance and vendor billing • Managing transport, canteen, pest control, and waste management services • Monitoring hygiene standards within facility premises • Managing stationery and operational supplies Administrative teams support the operational efficiency of pharmaceutical manufacturing facilities. Eligibility / Qualifications Promea Therapeutics is seeking candidates with relevant academic backgrounds in life sciences, pharmacy, engineering, and management. Required Educational Background B.Sc Chemistry, B.Sc Biotechnology, M.Sc Chemistry, M.Sc Biotechnology, B.Pharm, M.Pharm, B.Tech Biotechnology, M.Tech Biotechnology, B.Com, MBA, Diploma Mechanical Engineering, Diploma Electrical Engineering, ITI Technical Trades These academic programs provide the knowledge required for pharmaceutical production, biotechnology processes, and manufacturing operations. Experience Requirements Admin Supervisor 1 – 3 years Warehouse Junior Executive 0 – 3 years LVP FFS Operator Freshers eligible LVP Production Junior Executive Freshers eligible Biologics Production Junior Executive Freshers eligible Required Skills Ideal candidates should demonstrate: • Knowledge of GMP and GDP pharmaceutical guidelines • Understanding of pharmaceutical manufacturing processes • Ability to maintain production documentation • Familiarity with laboratory or manufacturing equipment • Strong teamwork and communication skills Candidates interested in biopharmaceutical manufacturing and sterile production technologies are strongly encouraged to apply. Location & Salary Job Location Promea Therapeutics Pvt. Ltd. Medical Devices Park Sultanpur, Ameenpur Sangareddy District Telangana – 502319 The facility is located within one of India’s largest pharmaceutical and biotechnology manufacturing clusters. Salary Salary packages depend on candidate qualifications, technical expertise, and company policies. Entry‑level pharmaceutical production roles typically include training programs and career development opportunities within the biotechnology sector. Application Process Interested candidates can apply by sending their updated resume to the official HR email addresses. Send your CV to: Saibaba.akana@promea.in or careers@promea.in For further details candidates may contact: Mobile: 9100554457 9100554484 Applicants should include the following details in their email application: • Full name • Qualification • Year of graduation • Total experience • Current location Shortlisted candidates will be contacted by the recruitment team for further selection processes. Why Build a Career in Biopharmaceutical Manufacturing Biopharmaceutical manufacturing is one of the fastest growing sectors within the global healthcare industry. Companies involved in biologics and sterile injectable production require highly trained professionals who understand bioprocessing technologies, sterile manufacturing systems, and pharmaceutical quality compliance frameworks. Professionals working in biotechnology manufacturing gain expertise in areas such as: • Biologics production technology • Downstream bioprocessing • Sterile injectable manufacturing • Pharmaceutical GMP compliance • Biotechnology process development These skills are highly valued across biotechnology companies, pharmaceutical manufacturers, contract manufacturing organizations (CMOs), and global healthcare companies. Career progression opportunities include: • Biologics Production Executive • Pharmaceutical Manufacturing Specialist • Bioprocess Engineer • Quality Assurance Manager • Biotechnology Plant Operations Manager With increasing global demand for biologic medicines, professionals trained in biopharmaceutical manufacturing technologies remain in strong demand worldwide. Frequently Asked Questions (FAQs) Who can apply for Promea Therapeutics jobs? Candidates with B.Sc, M.Sc, B.Pharm, M.Pharm, B.Tech Biotechnology, ITI, Diploma Engineering, B.Com, or MBA qualifications can apply depending on the department. Are freshers eligible for these roles? Yes. Several positions including LVP Production, Biologics Production, and BFS Operator roles are open for fresh graduates. What manufacturing technologies are used at the facility? The facility uses technologies such as Blow‑Fill‑Seal (BFS), biologics purification systems, filtration systems, and sterile manufacturing processes. Where is the job location? The positions are based at Promea Therapeutics manufacturing facility located in Medical Devices Park, Sangareddy, Telangana. How can candidates apply for these positions? Candidates can send their updated resume to the official HR email addresses mentioned in the job announcement. Job Summary Company Promea Therapeutics Pvt. Ltd. Vacancies LVP Production Jr Executive, Biologics Production Jr Executive, Warehouse Jr Executive, BFS Operator, Admin Supervisor Required Education BSc, MSc, BPharm, MPharm, BTech Biotechnology, Diploma, ITI, BCom, MBA Experience Freshers to 3 Years [...] Read more...

IQVIA Fresher Recruitment – Associate Consultant for all Lifesciences candidates

March 10, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Pharma Freshers Eye IQVIA Associate Consultant Opportunity A new opportunity at IQVIA is drawing attention from pharmacy and life-science graduates across India. The global healthcare analytics and consulting giant is hiring Associate Consultants for its consulting and commercial strategy team, offering a hybrid work opportunity for candidates interested in pharmaceutical market research and healthcare consulting. For B.Pharm and M.Pharm graduates aiming to move beyond traditional manufacturing roles, this opening represents a different path inside the life-sciences industry. Instead of laboratory or plant work, the role focuses on healthcare analytics, pharmaceutical market strategy, and consulting projects that guide global drug development and commercialization decisions. The position is based in Tamil Nadu, India, and offers professionals the chance to work with pharmaceutical companies, biotechnology firms, and healthcare organizations through data-driven consulting projects. Company Overview IQVIA is one of the world’s largest providers of clinical research services, healthcare analytics, and pharmaceutical consulting solutions. The company supports drug development, commercialization strategies, and healthcare intelligence for life sciences organizations globally. Formed through the merger of IMS Health and Quintiles, IQVIA combines real-world data, advanced analytics, and consulting expertise to help pharmaceutical companies accelerate innovation. Its services support clinical trials, regulatory strategy, commercial launches, and healthcare decision-making. With operations in more than 100 countries, IQVIA plays a critical role in helping pharmaceutical companies bring innovative therapies to patients faster. Professionals working at the company gain exposure to global healthcare markets, commercial strategy consulting, and advanced healthcare data intelligence platforms. Job Role and Responsibilities The Associate Consultant position is designed for professionals interested in healthcare consulting, pharmaceutical market analysis, and strategic advisory services. Selected candidates will contribute to consulting projects that support pharmaceutical companies in understanding market dynamics, launching products, and optimizing healthcare strategies. Key responsibilities include: Support the design and development of healthcare technology and consulting solutions Analyze pharmaceutical market trends and generate insights for life sciences clients Conduct healthcare market research to identify product opportunities and business needs Assist in defining product specifications, pricing strategies, and product launch plans Collaborate with internal teams and cross-functional stakeholders on consulting projects Prepare reports, data analysis summaries, and presentations for client engagements Participate in workshops and strategy sessions with pharmaceutical clients Assist senior consultants in proposal writing and business development activities Develop knowledge of healthcare consulting methodologies and industry trends Maintain strong collaboration with global project teams and client stakeholders These responsibilities expose professionals to high-level decision making within pharmaceutical companies, biotechnology firms, and healthcare organizations. Eligibility and Educational Qualifications IQVIA is looking for candidates with academic backgrounds in life sciences, healthcare, business, or analytical disciplines. Eligible educational qualifications include: B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Biomedical Sciences, Healthcare Management, Economics, Business Administration, MBA Healthcare Management, Statistics, Data Analytics Additional requirements include: Bachelor’s or Master’s degree in Life Sciences, Economics, or Business related disciplines PhD candidates with commercial healthcare experience may also apply Strong analytical and problem-solving skills Ability to work with healthcare data and generate actionable insights Excellent communication and presentation skills Knowledge of pharmaceutical industry trends and healthcare markets Effective collaboration and project management abilities Candidates who understand healthcare market dynamics, pharmaceutical commercialization strategies, or healthcare consulting frameworks will have an advantage in this role. Location and Work Mode The Associate Consultant role is based in Tamil Nadu, India, with a hybrid working model that allows professionals to balance office collaboration with remote flexibility. Application Process Interested candidates can apply directly through the official IQVIA careers portal. Application Link: https://jobs.iqvia.com/en/jobs/R1526444-0 Applicants should ensure that all information provided in their application is accurate and complete. IQVIA maintains strict recruitment integrity policies and follows a zero-tolerance approach toward candidate fraud or misrepresentation during the hiring process. Candidates selected for the next stage of recruitment may be invited to interviews that evaluate analytical thinking, consulting capabilities, and knowledge of the pharmaceutical industry. Frequently Asked Questions Who can apply for the IQVIA Associate Consultant role? Candidates with degrees in life sciences, pharmacy, economics, business administration, or healthcare management can apply for this consulting opportunity. Is prior consulting experience required? While consulting experience is beneficial, candidates with strong analytical skills and knowledge of the pharmaceutical industry may also be considered. What type of work does an Associate Consultant perform? The role focuses on healthcare consulting, pharmaceutical market research, healthcare data analysis, and supporting strategic advisory projects for life sciences companies. Is the role remote or office based? The position follows a hybrid working model, allowing a mix of remote work and office collaboration. How can candidates apply? Applicants can submit their application through the official IQVIA careers website using the provided link. Job Summary Company IQVIA Vacancies Associate Consultant Required Education B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Economics, Business Administration, MBA Healthcare, Statistics Experience Freshers to Experienced Candidates (Preferred Industry Exposure) Department Healthcare Consulting / Pharmaceutical Market Strategy Work Mode Hybrid Location Tamil Nadu, India Application Apply through IQVIA Career Portal [...] Read more...

Elysium Hiring Production Officer

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BPharm MSc Fresher Production Officer Jobs | Elysium Pharma Vadodara BPharm, MPharm, BSc, MSc fresher vacancies at Elysium Pharmaceutical Ltd Vadodara for Production Officer roles. Elysium Pharmaceutical Ltd. has announced fresh hiring for Production Officer positions at its pharmaceutical manufacturing facility in Vadodara, Gujarat. This opportunity is designed for fresh graduates who want to start their careers in pharmaceutical production, manufacturing operations, and GMP-compliant drug manufacturing environments. The pharmaceutical manufacturing industry requires skilled professionals who can support safe, compliant, and efficient production of medicines. Entry-level production roles provide the foundation for building long-term careers in pharmaceutical manufacturing, regulatory compliance, process validation, and production management. Elysium Pharmaceutical Ltd. is inviting applications from B.Pharm, M.Pharm, B.Sc, and M.Sc graduates who want to gain practical exposure in pharmaceutical production units handling tablets, injectables, and softgel dosage forms. These dosage forms represent some of the most widely used pharmaceutical delivery systems in modern healthcare. Candidates selected for this role will work closely with experienced production teams, quality assurance professionals, and regulatory compliance specialists. The role provides exposure to Good Manufacturing Practices (GMP), Standard Operating Procedures (SOP), pharmaceutical batch documentation systems, and controlled manufacturing processes used in global pharmaceutical manufacturing facilities. For graduates seeking a strong start in the pharmaceutical sector, working in production operations allows them to understand the full lifecycle of drug manufacturing from raw material handling to final product packaging and regulatory documentation. Company Overview Elysium Pharmaceutical Ltd. is a pharmaceutical manufacturing company engaged in the production and distribution of high-quality pharmaceutical formulations. The organization focuses on delivering reliable healthcare products that meet strict pharmaceutical regulatory standards. The pharmaceutical industry operates under highly regulated conditions to ensure that medicines are safe, effective, and consistently manufactured. Companies like Elysium Pharmaceutical invest heavily in modern manufacturing technologies, quality laboratories, and regulatory compliance systems to meet global healthcare standards. Elysium Pharmaceutical’s manufacturing operations support various dosage forms including tablets, injectable formulations, and softgel capsules. Each dosage form requires specialized manufacturing processes, validated production procedures, and rigorous quality control systems. The company follows internationally recognized pharmaceutical regulatory frameworks such as: • Good Manufacturing Practices (GMP) • Quality Management Systems (QMS) • Pharmaceutical documentation and batch record systems • Regulatory compliance guidelines These systems ensure that pharmaceutical products manufactured at the facility meet both domestic and international healthcare standards. Working with Elysium Pharmaceutical allows young professionals to gain experience in pharmaceutical production technology, regulatory quality systems, manufacturing process management, and pharmaceutical compliance frameworks. Job Role & Responsibilities The Production Officer (Fresher) role involves supporting pharmaceutical manufacturing operations while learning the regulatory and operational requirements of pharmaceutical production environments. Manufacturing Operations Support Production officers assist in executing manufacturing activities according to approved production procedures. Key responsibilities include: • Assisting production teams in executing manufacturing batches • Supporting pharmaceutical production processes for tablets, injectables, or softgel capsules • Monitoring manufacturing equipment and production parameters • Following Standard Operating Procedures (SOPs) during production operations • Supporting supervisors during batch manufacturing activities These responsibilities ensure that pharmaceutical products are manufactured safely and consistently. Compliance with GMP Guidelines Pharmaceutical manufacturing requires strict compliance with Good Manufacturing Practices (GMP). Key responsibilities include: • Ensuring production operations comply with GMP standards • Maintaining cleanliness and hygiene within manufacturing areas • Following approved production and documentation procedures • Supporting production teams during audits and inspections GMP compliance ensures that pharmaceutical products maintain quality, safety, and regulatory approval. Production Documentation Accurate documentation is a critical requirement in pharmaceutical manufacturing because regulatory agencies closely review manufacturing records. Key responsibilities include: • Maintaining batch production documentation • Supporting documentation related to manufacturing operations • Ensuring accurate data entry in production records • Maintaining compliance with documentation procedures These records help maintain traceability and regulatory transparency in pharmaceutical production. Cross-Department Coordination Production teams collaborate with multiple departments to ensure smooth manufacturing operations. Key responsibilities include: • Coordinating with Quality Assurance teams for compliance monitoring • Working with maintenance teams for equipment readiness • Supporting warehouse teams for raw material handling • Assisting supervisors in resolving production challenges Collaboration between departments ensures efficient pharmaceutical manufacturing operations. Eligibility / Qualifications Elysium Pharmaceutical Ltd. is seeking fresh graduates who want to build careers in pharmaceutical manufacturing and production management. Required Educational Background B.Pharm, M.Pharm, B.Sc Chemistry, B.Sc Biotechnology, B.Sc Microbiology, M.Sc Chemistry, M.Sc Biotechnology, M.Sc Microbiology These academic programs provide foundational knowledge in pharmaceutical sciences, chemical processes, and biological systems relevant to pharmaceutical manufacturing. Experience Requirement Freshers are eligible to apply. This role is specifically designed for candidates beginning their careers in pharmaceutical manufacturing. Required Skills Ideal candidates should demonstrate: • Basic knowledge of pharmaceutical production processes • Understanding of GMP guidelines • Attention to detail and quality standards • Strong communication and teamwork skills • Willingness to work in manufacturing environments Candidates interested in pharmaceutical manufacturing operations and production process management are strongly encouraged to apply. Location & Salary Job Location Elysium Pharmaceutical Ltd. Vadodara Gujarat, India Vadodara is one of India’s major pharmaceutical and chemical manufacturing hubs and hosts several pharmaceutical companies and research organizations. Salary Salary packages for fresh graduates depend on company policies and training structures. Entry-level pharmaceutical production roles generally include structured training programs and career development opportunities. Application Process Interested candidates can apply by submitting their updated resume to the company’s HR department. Send your CV to: aman.kumar@elysiumpharma.com Applicants should include the following details in their application email: • Full name • Educational qualification • Year of graduation • Current location • Contact number Shortlisted candidates may be contacted by the HR team for further interview rounds. Why Start a Career in Pharmaceutical Production Pharmaceutical production is one of the most important operational functions in the healthcare industry. Production professionals are responsible for ensuring that medicines are manufactured safely, efficiently, and according to regulatory standards. Professionals working in pharmaceutical manufacturing gain exposure to key industry areas including: • Drug manufacturing processes • Pharmaceutical quality compliance systems • GMP regulatory standards • Production process optimization • Pharmaceutical supply chain operations Early exposure to pharmaceutical manufacturing operations helps professionals build strong technical skills that can lead to long-term careers in pharmaceutical companies. Typical career progression in pharmaceutical production includes: • Production Officer • Production Executive • Manufacturing Supervisor • Production Manager • Plant Operations Manager With increasing global demand for medicines, professionals trained in pharmaceutical manufacturing and GMP-compliant production systems remain highly valuable across pharmaceutical companies worldwide. Frequently Asked Questions (FAQs) Who can apply for the Elysium Pharmaceutical Production Officer role? Fresh graduates with B.Pharm, M.Pharm, B.Sc, or M.Sc qualifications in relevant fields can apply. Is prior pharmaceutical experience required? No. The role is designed for freshers who want to start careers in pharmaceutical manufacturing. What departments will the production officer work with? Production officers typically work with Quality Assurance, Quality Control, Warehouse, and Engineering teams. What dosage forms are manufactured at the facility? The company manufactures tablets, injectable formulations, and softgel capsules. How can candidates apply? Candidates can apply by sending their updated resume to the official HR email mentioned in the job announcement. Job Summary Company Elysium Pharmaceutical Ltd. Vacancies Production Officer Required Education B.Pharm, M.Pharm, B.Sc, M.Sc Experience Freshers [...] Read more...

Kwality Hiring QC, QA, Micro & Engineering

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BPharm MSc QC QA Jobs | Kwality Pharma Amritsar BPharm, MPharm, MSc pharma vacancies at Kwality Pharmaceuticals Amritsar for QC, QA, Micro & Engineering roles. Kwality Pharmaceuticals Ltd. has announced multiple hiring opportunities across Quality Control, Microbiology, Quality Assurance, and Engineering departments at its pharmaceutical manufacturing facility located in Amritsar, Punjab. The company is actively seeking professionals from pharmaceutical sciences, biotechnology, and engineering backgrounds who want to build long-term careers in regulated pharmaceutical manufacturing. These openings are part of the company’s expansion within specialized manufacturing segments such as hormone block pharmaceutical production, which requires strict compliance with regulatory standards, advanced containment technologies, and highly controlled manufacturing processes. Professionals selected for these roles will contribute to ensuring high-quality pharmaceutical products that meet international healthcare standards. Candidates with B.Pharm, M.Pharm, MSc, B.Tech Biotechnology, Diploma Engineering, and ITI technical qualifications are eligible to apply depending on the department. Both fresh graduates and experienced professionals with up to six years of pharmaceutical industry experience are encouraged to apply. Working in pharmaceutical manufacturing provides exposure to highly specialized operations including Good Manufacturing Practices (GMP), analytical quality testing, sterile manufacturing environments, documentation systems, regulatory inspections, and pharmaceutical plant engineering systems. These skills are critical in supporting the global supply of safe and effective medicines. Professionals joining Kwality Pharmaceuticals will have the opportunity to work with experienced teams, advanced pharmaceutical manufacturing infrastructure, and globally recognized quality systems that support international pharmaceutical markets. Company Overview Kwality Pharmaceuticals Ltd. is a well-established pharmaceutical company engaged in the development, manufacturing, and distribution of high-quality pharmaceutical products. The company has built a strong reputation for producing complex pharmaceutical molecules using advanced research capabilities and modern manufacturing technologies. The organization operates state-of-the-art pharmaceutical manufacturing infrastructure that supports production across multiple dosage forms and therapeutic segments. These facilities follow strict global regulatory frameworks to ensure medicines manufactured meet international quality standards. Pharmaceutical companies operating in highly regulated markets must comply with several international regulatory frameworks, including: • Good Manufacturing Practices (GMP) • Good Laboratory Practices (GLP) • Quality Management Systems (QMS) • International regulatory guidelines and pharmaceutical inspection standards Kwality Pharmaceuticals focuses heavily on innovation, research, and manufacturing excellence. The company’s emphasis on research and development allows it to manufacture complex pharmaceutical compounds used in modern medicine. The company’s manufacturing facility located in Village Nag Kalan, Majitha Road, Amritsar supports large-scale pharmaceutical production while maintaining strict quality systems. The facility includes quality control laboratories, microbiology laboratories, engineering utilities, and pharmaceutical manufacturing lines designed to meet global regulatory requirements. By joining Kwality Pharmaceuticals, professionals gain exposure to pharmaceutical research-driven manufacturing, advanced quality control systems, regulatory documentation processes, and global pharmaceutical supply chain operations. Job Role & Responsibilities Kwality Pharmaceuticals is recruiting professionals across multiple departments that support pharmaceutical manufacturing and quality operations. Quality Control (QC) Quality Control professionals are responsible for performing laboratory testing to ensure pharmaceutical materials and finished products meet strict quality specifications. Key responsibilities include: • Conducting analytical testing of pharmaceutical samples • Preparing and reviewing analytical documentation • Ensuring compliance with Good Laboratory Practices (GLP) • Reviewing Standard Operating Procedures (SOPs) • Preparing specifications and standard testing procedures (STP) • Supporting stability testing and analytical method verification QC laboratories ensure pharmaceutical products meet purity, potency, and safety standards required by regulatory agencies. Microbiology Department Microbiology teams ensure that pharmaceutical manufacturing environments remain free from microbial contamination. Key responsibilities include: • Performing microbiological analysis of environmental samples • Supporting environmental monitoring programs • Preparing microbiology documentation and laboratory records • Reviewing SOPs and specifications for microbiological testing • Ensuring microbial control within pharmaceutical production areas Microbiological quality monitoring is particularly important in pharmaceutical manufacturing facilities producing sterile or highly sensitive drug products. Quality Assurance (QA) Quality Assurance professionals ensure that pharmaceutical manufacturing operations comply with regulatory standards and internal quality systems. Key responsibilities include: • Monitoring GMP compliance across production operations • Supporting equipment and utility qualification processes • Maintaining quality documentation systems • Reviewing SOPs, protocols, and reports • Supporting internal audits and regulatory inspection readiness • Ensuring compliance with pharmaceutical Quality Management Systems (QMS) QA teams ensure that medicines are manufactured consistently according to approved regulatory procedures. Engineering Department Engineering teams support pharmaceutical plant infrastructure, utilities, and equipment maintenance. Key responsibilities include: • Maintaining plant utility systems • Supporting electrical maintenance operations • Maintaining HVAC systems and water systems • Performing preventive maintenance activities • Supporting plant troubleshooting and equipment repairs Engineering professionals play a vital role in ensuring uninterrupted pharmaceutical manufacturing operations. Eligibility / Qualifications Kwality Pharmaceuticals is seeking professionals with academic backgrounds in pharmaceutical sciences, biotechnology, chemistry, and engineering. Required Educational Background B.Pharm, M.Pharm, MSc Chemistry, MSc Microbiology, MSc Biotechnology, B.Tech Biotechnology, B.Tech Engineering, Diploma Engineering, ITI Electrician, ITI Technical Trades These qualifications provide the scientific and technical foundation required for pharmaceutical manufacturing and quality operations. Experience Requirement Quality Control 2 to 6 years of pharmaceutical QC experience Microbiology 2 to 6 years of microbiology laboratory experience Quality Assurance Fresher to 6 years of experience in pharmaceutical QA functions Engineering 2 to 6 years of experience in plant utilities, maintenance, electrical systems, HVAC systems, and water systems Required Skills Candidates should demonstrate the following professional skills: • Knowledge of pharmaceutical GMP standards • Experience with pharmaceutical documentation systems • Understanding of analytical testing or microbiological testing • Familiarity with plant engineering systems • Ability to work in regulated pharmaceutical manufacturing environments Professionals with experience in hormone block pharmaceutical manufacturing environments may receive preference due to the specialized nature of these production facilities. Location & Salary Job Location Kwality Pharmaceuticals Ltd. Village Nag Kalan Majitha Road Amritsar – 143601 Punjab, India Amritsar hosts several pharmaceutical and healthcare manufacturing companies and provides strong opportunities for professionals working in pharmaceutical production and quality functions. Salary Salary packages depend on candidate qualifications, technical experience, and role responsibilities. Pharmaceutical companies typically offer competitive salary structures along with additional benefits for skilled professionals working in quality and manufacturing functions. Application Process Interested candidates can apply by sending their updated resumes through the official recruitment channels. Email your CV to: career@kwalitypharma.com Candidates may also contact the HR team through the following numbers: +91 98374 54653 +91 9878020047 Applicants are encouraged to include the following details in their email application: • Full name • Educational qualification • Total years of experience • Current company (if applicable) • Current salary and expected salary • Notice period Shortlisted candidates may be contacted for interview rounds conducted by the company’s recruitment team. Why Build a Career in Pharmaceutical Manufacturing The pharmaceutical industry continues to expand globally as healthcare demand increases. Professionals working in pharmaceutical manufacturing gain exposure to advanced technologies and regulatory frameworks that ensure medicines are produced safely and consistently. Key areas of professional development include: • Pharmaceutical regulatory compliance • Analytical laboratory testing • Microbiological quality monitoring • Pharmaceutical plant engineering systems • Global pharmaceutical quality standards Professionals trained in these areas are highly valued across pharmaceutical companies, contract manufacturing organizations, and biotechnology firms worldwide. Typical career progression in pharmaceutical manufacturing may include: • Quality Control Executive • Quality Assurance Manager • Pharmaceutical Microbiology Specialist • Plant Engineering Manager • Pharmaceutical Operations Manager The combination of technical knowledge and regulatory expertise makes pharmaceutical professionals essential contributors to global healthcare systems. Frequently Asked Questions (FAQs) Who can apply for Kwality Pharmaceuticals jobs? Candidates with B.Pharm, M.Pharm, MSc, B.Tech Biotechnology, engineering diplomas, or ITI technical qualifications can apply depending on the department. What departments are currently hiring? The company is hiring for Quality Control, Microbiology, Quality Assurance, and Engineering departments. Is pharmaceutical industry experience required? Most roles require 2–6 years of experience, while some QA positions are open to fresh graduates. Where is the job location? The positions are based at Kwality Pharmaceuticals manufacturing facility located in Amritsar, Punjab. How can candidates apply for these positions? Interested applicants can send their updated resume to the official recruitment email provided by the company. Job Summary Company Kwality Pharmaceuticals Ltd. Vacancies Quality Control Officer, Microbiology Officer, QA Executive, Engineering Technician Required Education B.Pharm, M.Pharm, MSc, B.Tech Biotechnology, Diploma Engineering, ITI Experience Fresher to 6 Years [...] Read more...

Apprentices Opportunity for B Pharm, Microbiology, Biote – QA, QC, Micro & Production – Gufic Biosciences

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Gufic Biosciences Walk‑In Drive for QA, QC, Microbiology & Production Apprentices Fresh pharmacy and life science graduates looking to begin their careers in pharmaceutical manufacturing now have a strong opportunity. Gufic Biosciences Limited has announced a walk‑in interview drive for Apprentice roles across QA, QC, Microbiology, and Production departments at its major injectable manufacturing facility in Indore. For B.Pharm and B.Sc graduates searching for their first pharmaceutical industry role, this hiring drive offers practical exposure inside one of the world’s largest lyophilized injectable manufacturing plants. Early industry experience in regulated pharmaceutical facilities helps fresh graduates understand GMP operations, quality systems, and large‑scale drug manufacturing. With injectable medicines becoming increasingly important in modern healthcare, pharmaceutical companies are expanding skilled technical teams to support production and quality control operations. Company Overview Gufic Biosciences Limited is a globally recognized pharmaceutical company specializing in injectable formulations and lyophilized drug products. The company has built a strong reputation in sterile injectable manufacturing and exports pharmaceutical products to several international markets. The organization operates advanced pharmaceutical manufacturing facilities that follow strict regulatory guidelines such as Good Manufacturing Practices and international quality standards. Through continuous investment in research, manufacturing technology, and regulatory compliance, Gufic Biosciences continues to strengthen its presence in global pharmaceutical markets. The company’s Indore facility is known as one of the largest lyophilized injectable manufacturing plants in the world, supporting large‑scale production of critical injectable medicines used in hospitals and healthcare systems. Career Outlook for Pharmaceutical Manufacturing & Quality Professionals in 2026 The pharmaceutical manufacturing sector is expected to grow significantly through 2026 as global demand for injectable medicines and complex drug formulations increases. Companies manufacturing sterile injectables require highly trained professionals in quality assurance, quality control, microbiology, and production operations. Fresh graduates who start their careers through apprenticeship programs gain valuable hands‑on training in GMP manufacturing environments. This early exposure to pharmaceutical operations helps build strong technical skills in quality testing, sterile manufacturing processes, and regulatory compliance. Professionals who begin their careers in QA, QC, microbiology, or production departments often progress into roles such as Quality Assurance Executive, Quality Control Analyst, Production Executive, Microbiology Scientist, or Manufacturing Supervisor in pharmaceutical companies. Job Role & Responsibilities Selected candidates will join as Apprentices and receive structured training within the pharmaceutical manufacturing environment. Key responsibilities during the apprenticeship may include: Supporting quality assurance activities within pharmaceutical manufacturing operations Assisting in quality control testing and laboratory documentation Participating in microbiology laboratory testing and environmental monitoring Supporting production activities for sterile injectable manufacturing Maintaining documentation according to GMP and SOP guidelines Learning pharmaceutical manufacturing processes and regulatory compliance requirements This training provides fresh graduates with real industry exposure and technical knowledge required for long‑term pharmaceutical careers. Eligibility / Qualifications Candidates interested in attending the walk‑in interview should meet the following criteria: Bachelor of Pharmacy (B.Pharm) degree Bachelor of Science in Microbiology or Biotechnology Freshers are eligible to apply Relevant education backgrounds include: B.Pharm, B.Sc Microbiology, B.Sc Biotechnology, B.Sc Life Sciences, B.Sc Biochemistry. Apprenticeship Details Designation: Apprentice Departments: Quality Assurance (QA), Quality Control (QC), Microbiology, Production Duration: 1 Year Apprenticeship Program This program allows fresh graduates to gain hands‑on pharmaceutical manufacturing experience while learning industry best practices and regulatory compliance standards. Location & Facilities Location: Pithampur, Indore, Madhya Pradesh Interview Venue: Gufic Biosciences Limited Plot No. 48, Smart Industrial Park, Natrip Pithampur, Dhar – 454775 Bus transportation facility will be available from Indore for candidates attending the interview. Walk‑In Interview Details Date: Saturday, 14 March 2026 Time: 10:00 AM to 04:00 PM Immediate joiners may be given preference during the selection process. Candidates are advised to carry updated resumes, academic documents, and identification proof while attending the interview. Application Process Interested candidates can directly attend the walk‑in interview at the venue mentioned above. For transportation queries, candidates may contact: Phone: 77719 90089 Early arrival is recommended due to high participation in pharmaceutical fresher hiring drives. Frequently Asked Questions Who can attend the Gufic Biosciences walk‑in interview? B.Pharm graduates and B.Sc graduates in Microbiology or Biotechnology can attend the interview. Is this opportunity open for freshers? Yes. The apprenticeship program is specifically designed for fresh graduates entering the pharmaceutical industry. Which departments are hiring apprentices? Quality Assurance, Quality Control, Microbiology, and Production departments. What career opportunities exist after apprenticeship training? Candidates may progress into roles such as QA Executive, QC Analyst, Microbiologist, Production Executive, or Pharmaceutical Manufacturing Specialist. Summary Category Details Company Gufic Biosciences Limited Vacancies Apprentice – QA, QC, Microbiology, Production Required Education B.Pharm, B.Sc Microbiology, B.Sc Biotechnology Experience Freshers Eligible Location Pithampur, Indore, Madhya Pradesh Duration 1 Year Apprenticeship [...] Read more...

B Pharma Fresher Alert: Glumex Opens Maintenance Role with Housing

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Glumex Pharmaceuticals Hiring Maintenance Executive for B.Pharm Freshers in Wada Pharmacy graduates searching for their first role in the pharmaceutical manufacturing industry now have a new opportunity. Glumex Pharmaceuticals Pvt Ltd has announced hiring for Maintenance Executive positions at its Wada facility in Palghar, Maharashtra, with company accommodation available for selected candidates. For B.Pharm freshers looking to enter the pharmaceutical production environment, this role offers practical exposure to manufacturing operations, equipment maintenance, and regulated pharmaceutical facility management. Early career roles like this allow pharmacy graduates to understand how pharmaceutical plants operate while building experience in GMP-compliant environments. As India’s pharmaceutical manufacturing sector continues expanding, companies are actively recruiting young professionals who can support equipment reliability, production continuity, and quality-driven manufacturing operations. Company Overview Glumex Pharmaceuticals Pvt Ltd is an emerging pharmaceutical manufacturing organization focused on producing high-quality pharmaceutical products in compliance with industry standards. The company operates manufacturing facilities designed to meet regulatory expectations required for pharmaceutical production and quality assurance. Like many growing pharmaceutical manufacturers in India, Glumex focuses on maintaining strict quality control processes, Good Manufacturing Practice compliance, and operational efficiency in its production facilities. These practices ensure that medicines manufactured at the facility meet safety, quality, and regulatory requirements before reaching patients. Companies operating pharmaceutical plants require trained professionals who understand the importance of equipment maintenance, process reliability, and regulatory compliance in pharmaceutical manufacturing environments. Career Outlook for Pharmaceutical Manufacturing & Safety Science Professionals in 2026 The pharmaceutical manufacturing industry is expected to grow steadily through 2026 as global demand for medicines continues to increase. With India playing a major role in global generic drug production, pharmaceutical companies are investing heavily in manufacturing infrastructure and production technology. Maintenance professionals play a critical role in ensuring that pharmaceutical production lines operate smoothly without interruption. Equipment reliability, process safety, and regulatory compliance depend heavily on well-managed maintenance operations. Pharmacy graduates who begin their careers in manufacturing support roles often gain deep knowledge of pharmaceutical equipment, validation systems, and GMP processes. Over time, professionals may advance into positions such as Production Executive, Engineering Coordinator, Validation Specialist, Manufacturing Supervisor, or Plant Operations Manager. Experience in pharmaceutical plant operations also opens doors to roles in quality assurance, regulatory compliance, and manufacturing technology management. Job Role & Responsibilities The Maintenance Executive will support the smooth functioning of pharmaceutical manufacturing equipment and facility systems. Key responsibilities include: Assist in maintaining pharmaceutical manufacturing equipment and plant utilities Support routine inspection and preventive maintenance activities Ensure production machinery operates efficiently during manufacturing cycles Identify technical issues and coordinate timely repairs or troubleshooting Maintain maintenance documentation according to pharmaceutical SOPs Work closely with production teams to avoid downtime in manufacturing operations Ensure maintenance activities comply with Good Manufacturing Practice guidelines Support facility teams in maintaining safe and compliant working conditions This role helps ensure continuous pharmaceutical production while maintaining equipment reliability and regulatory compliance. Eligibility / Qualifications Candidates interested in this pharmaceutical manufacturing opportunity should meet the following criteria: Bachelor of Pharmacy (B.Pharm) degree Freshers are eligible to apply Interest in pharmaceutical manufacturing operations and maintenance systems Basic understanding of GMP practices in pharmaceutical production Strong problem-solving ability and willingness to work in plant environments Relevant education backgrounds may include: B.Pharm, M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Analysis, B.Sc Chemistry, B.Sc Pharmaceutical Sciences. Location & Salary Location: Wada, Palghar District, Maharashtra, India Accommodation: Company accommodation is available for selected candidates working at the facility. Application Process Interested candidates can apply by sending their updated resume to the recruitment email provided below. Email Application: admin@glumex.in Candidates should mention their qualification and interest in pharmaceutical manufacturing roles when submitting their applications. Early applications are recommended as fresher opportunities in pharmaceutical manufacturing facilities often receive a large number of applications. Frequently Asked Questions Who can apply for the Glumex Maintenance Executive role? B.Pharm graduates and pharmacy freshers interested in pharmaceutical manufacturing operations can apply. Is accommodation provided for employees? Yes. Company accommodation is available for candidates selected for the position. Is this role suitable for fresh pharmacy graduates? Yes. The company is open to hiring B.Pharm freshers who want to start careers in pharmaceutical plant operations. What career growth opportunities exist in pharmaceutical manufacturing? Professionals may progress into roles such as Production Executive, Validation Engineer, Plant Supervisor, Manufacturing Manager, or Quality Assurance Specialist. Summary Category Details Company Glumex Pharmaceuticals Pvt Ltd Vacancies Maintenance Executive Required Education B.Pharm Experience Freshers Eligible Location Wada, Palghar, Maharashtra Department Manufacturing / Maintenance [...] Read more...

Syngene Hiring Pharmacist for Clinical Trial Supply Management in Bangalore

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Syngene Hiring Clinical Trial Pharmacist in Bangalore for M.Pharm Global contract research and development organization Syngene International has announced hiring for the position of Pharmacist within its Biometrics division in Bangalore. The role focuses on clinical trial supply management and investigational product handling, making it a valuable opportunity for pharmacy professionals interested in clinical research operations. As pharmaceutical companies continue expanding global clinical trials, the demand for pharmacists who understand investigational product (IP) management and regulatory compliance is growing rapidly. This position allows professionals to work closely with clinical trial teams and contribute to drug development programs that ultimately lead to new therapies reaching patients. For pharmacy graduates looking to move beyond traditional retail or hospital pharmacy roles, clinical trial pharmacy operations offer a highly specialized career path in the pharmaceutical research industry. Company Overview Syngene International Ltd. is a globally recognized contract research, development, and manufacturing organization (CRDMO). Established in 1993, the company provides integrated scientific services to pharmaceutical, biotechnology, nutrition, animal health, and consumer goods companies worldwide. The organization collaborates with several leading global pharmaceutical companies including Bristol‑Myers Squibb, Baxter, Amgen, GlaxoSmithKline, Merck KGaA, and Herbalife. Through its advanced research facilities and scientific expertise, Syngene supports clients in accelerating drug discovery, development, and commercialization. With thousands of scientists and research professionals working across multiple disciplines, the company plays a crucial role in improving research productivity and reducing the time required for pharmaceutical innovation. Career Outlook for Clinical Supply & Safety Science Professionals in 2026 Clinical trial supply management is becoming an increasingly critical function within pharmaceutical research organizations. By 2026, pharmaceutical companies and contract research organizations are expected to invest heavily in clinical trial logistics, investigational product management, and regulatory‑compliant drug supply chains. Pharmacists involved in clinical trial supply operations ensure that investigational medicinal products are handled, labeled, stored, and distributed according to strict regulatory standards. Their work directly supports clinical trials conducted across hospitals and research sites globally. Professionals who begin careers in clinical supply management can later progress into roles such as Clinical Trial Supply Manager, Clinical Operations Manager, Clinical Research Associate, or Regulatory Affairs Specialist. With increasing complexity in global clinical trials, expertise in investigational product management and regulatory compliance remains highly valuable. Job Role & Responsibilities The Pharmacist will play a central role in managing investigational medicinal products used in clinical trials conducted by Syngene. Key responsibilities include: Prepare protocol‑specific pharmacy plans and secondary labeling plans for clinical trials Manage receipt, verification, and storage of Investigational Medicinal Products (IMP) and Non‑Clinical Supplies (NCS) Perform labeling and relabeling activities including expiry extension and secondary labeling Coordinate supply and resupply of investigational products to clinical trial sites Ensure shipments maintain required temperature conditions during transportation Prepare shipment documentation and manage inventory of clinical trial supplies Maintain adequate supply of investigational products at research sites Conduct reconciliation and return processes for investigational products after study completion Witness destruction of unused investigational products according to approved procedures Maintain documentation for all clinical supply activities in compliance with regulatory guidelines These responsibilities ensure that clinical trials receive the correct drug supplies while maintaining strict quality and compliance standards. Compliance & Documentation Responsibilities The role requires strict adherence to international clinical research regulations and documentation practices. Responsibilities include: Ensure compliance with ICH‑GCP guidelines and local regulatory requirements Maintain standard operating procedures and clinical supply documentation Support internal and external audits related to clinical trial supply management Ensure calibration and maintenance of clinical supply unit instruments Accurate documentation and regulatory compliance are essential for maintaining data integrity and patient safety in clinical research studies. Eligibility / Qualifications Candidates interested in this clinical research pharmacist role should meet the following criteria: Master’s degree in Life Sciences or Pharmacology Strong knowledge of clinical trial supply management and investigational product handling Understanding of ICH‑GCP guidelines and Indian regulatory requirements Familiarity with Microsoft Office tools including Word, Excel, and PowerPoint Experience supporting audits and documentation processes Relevant education backgrounds may include: M.Pharm Pharmacology, M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Analysis, M.Sc Life Sciences, M.Sc Pharmacology. Location & Salary Location: Bangalore, Karnataka, India Application Process Interested candidates can apply through the official Syngene careers portal using the link below. Apply here: https://careers.syngeneintl.com/job/Bangalore-Pharmacist-KA-560100/1332430166/ Applicants should submit an updated resume highlighting experience in clinical trial pharmacy operations, regulatory compliance knowledge, and investigational product management. Early applications are recommended as clinical research roles in leading CRO organizations often receive strong interest from qualified candidates. Frequently Asked Questions Who can apply for the Syngene Pharmacist role? Candidates with a Master’s degree in Life Sciences or Pharmacology with knowledge of clinical trial operations can apply. What does a clinical trial pharmacist do? A clinical trial pharmacist manages investigational drug supplies, labeling, storage, and distribution to clinical research sites while ensuring compliance with regulatory guidelines. Is knowledge of ICH‑GCP required for this role? Yes. Understanding ICH‑GCP and regulatory requirements is important for professionals involved in clinical trial supply management. What career growth opportunities exist in clinical trial pharmacy roles? Professionals may progress into Clinical Supply Manager, Clinical Operations Specialist, Regulatory Affairs professional, or Clinical Research Associate roles. Summary Category Details Company Syngene International Ltd Vacancies Pharmacist – Clinical Trial Supply Management Required Education M.Pharm Pharmacology, M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Analysis, M.Sc Life Sciences Experience Experience in clinical trial supply or IP management preferred Location Bangalore, Karnataka Department Biometrics / Clinical Supply Management [...] Read more...

Global Calcium Hiring API Production Trainee

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now BSc Chemistry API Production Fresher Jobs | Global Calcium Hosur BSc Chemistry, Diploma Chemical, BTech Chemical fresher vacancies at Global Calcium API Production Hosur. Global Calcium Pvt. Ltd. is inviting applications from fresh graduates for API Production roles at its pharmaceutical manufacturing units located in SIPCOT Phase I, Hosur. This opportunity is designed for candidates who want to begin their careers in pharmaceutical and chemical manufacturing within a regulated Active Pharmaceutical Ingredient (API) production environment. Fresh graduates with qualifications in chemical engineering and chemistry often seek opportunities that provide practical exposure to industrial pharmaceutical processes. API manufacturing facilities provide such exposure by allowing professionals to work directly with chemical synthesis operations, industrial reactors, quality control systems, and pharmaceutical regulatory standards. Global Calcium is offering a structured entry point for 2024 and 2025 pass-out candidates who are eager to gain real-world experience in pharmaceutical manufacturing. Selected candidates will work alongside experienced production engineers and chemists while learning essential industry practices such as Good Manufacturing Practices (GMP), process safety protocols, and pharmaceutical production systems. For individuals interested in building long‑term careers in pharmaceutical manufacturing, this role provides an excellent foundation in API production operations, chemical process manufacturing, and pharmaceutical compliance systems used across the global pharma industry. Company Overview Global Calcium Pvt. Ltd. is a well‑known pharmaceutical manufacturing company specializing in the production of Active Pharmaceutical Ingredients (APIs) and mineral-based pharmaceutical ingredients used in healthcare formulations. The company supplies high‑quality pharmaceutical raw materials to pharmaceutical formulation manufacturers across domestic and international markets. API manufacturing companies play a critical role in the pharmaceutical industry because they produce the core chemical substances used to manufacture medicines such as tablets, capsules, syrups, and injections. Maintaining strict quality standards in API production is essential because the purity and quality of the active ingredient directly affect the safety and effectiveness of medicines. Global Calcium operates modern manufacturing facilities that follow strict Good Manufacturing Practices (GMP), pharmaceutical quality systems, and industrial safety standards. The company focuses on innovation, process optimization, and regulatory compliance to ensure its pharmaceutical products meet global quality requirements. The organization’s manufacturing units located in SIPCOT Industrial Park, Hosur, are equipped with advanced chemical manufacturing equipment, process reactors, quality testing laboratories, and industrial safety systems. These facilities support large-scale pharmaceutical manufacturing operations and provide an excellent learning environment for early‑career professionals. By joining Global Calcium, fresh graduates gain exposure to pharmaceutical manufacturing technology, chemical process engineering, industrial production management, and regulatory compliance practices required in the global pharmaceutical industry. Job Role & Responsibilities The API Production Fresher role focuses on supporting chemical manufacturing operations within pharmaceutical production units. Fresh graduates joining this role will work closely with senior production engineers and plant supervisors to learn how pharmaceutical active ingredients are manufactured safely and efficiently. API Production Operations Production teams are responsible for executing chemical synthesis and manufacturing operations that produce pharmaceutical active ingredients. Key responsibilities include: • Assisting in API manufacturing operations within the production plant • Supporting chemical synthesis processes and production batches • Monitoring production parameters and equipment performance • Maintaining batch manufacturing records and production documentation • Ensuring compliance with pharmaceutical Good Manufacturing Practices (GMP) • Supporting plant safety and operational procedures These activities ensure that pharmaceutical raw materials are manufactured according to strict quality standards required by global healthcare regulators. Learning Pharmaceutical Manufacturing Processes Freshers will receive training in pharmaceutical manufacturing systems and plant operations. Key learning areas include: • Chemical process manufacturing techniques • API synthesis and industrial reaction systems • Process safety protocols used in pharmaceutical plants • Pharmaceutical quality documentation systems • Equipment operation and plant production workflows Hands‑on exposure to these areas helps young professionals develop practical industry knowledge that cannot be gained through academic study alone. Quality and Safety Compliance Pharmaceutical manufacturing plants follow strict regulatory and safety standards to ensure both product quality and worker safety. Key responsibilities include: • Following GMP guidelines during production activities • Ensuring compliance with plant safety rules and chemical handling procedures • Supporting documentation practices required for regulatory compliance • Learning environmental health and safety practices used in chemical manufacturing plants These compliance practices help maintain pharmaceutical product integrity and safe manufacturing conditions. Team Collaboration Production professionals work in coordination with multiple departments within pharmaceutical manufacturing facilities. Responsibilities include: • Coordinating with quality control laboratories • Working with maintenance and engineering teams • Supporting warehouse teams for material handling • Assisting supervisors during production batch execution Collaborative teamwork ensures smooth pharmaceutical production operations and regulatory compliance. Eligibility / Qualifications Global Calcium Pvt. Ltd. is seeking motivated fresh graduates who want to begin careers in pharmaceutical and chemical manufacturing. Required Educational Background Diploma in Chemical Engineering, B.Sc Chemistry, B.Sc Industrial Chemistry, B.Tech Chemical Engineering, B.E Chemical Engineering Candidates who graduated in 2024 or 2025 are eligible to apply. Experience Requirement Fresher candidates only. Prior industry experience is not mandatory. Preferred Candidate Profile Ideal candidates should demonstrate: • Basic knowledge of chemical engineering or chemistry concepts • Interest in pharmaceutical manufacturing and API production • Strong attention to safety and quality procedures • Willingness to work in industrial manufacturing environments • Ability to learn and adapt to pharmaceutical production systems According to company hiring requirements, male candidates are preferred for this role due to plant operational conditions. Location & Salary Job Location Global Calcium Pvt. Ltd. Unit I & Unit II SIPCOT Phase I Hosur Tamil Nadu, India Hosur is one of the major industrial and pharmaceutical manufacturing regions in South India and hosts several chemical and pharmaceutical production companies. Salary Salary packages for fresh graduates typically depend on company policies, technical qualifications, and training programs. Entry‑level pharmaceutical production roles generally include structured training programs and career growth opportunities. Application Process Interested candidates can apply by sending their updated resumes to the HR department. Send your CV to: Roja.hr@globalcalciumpharma.com Applicants are encouraged to mention the following details in their email: • Full name • Qualification • Year of graduation • Contact number • Current location Candidates who demonstrate strong interest in pharmaceutical manufacturing and chemical production operations may be shortlisted for further interviews. Why Start Your Career in API Production API production is one of the most important sectors of the pharmaceutical industry because it involves manufacturing the chemical substances that form the foundation of medicines used worldwide. Professionals working in API manufacturing gain valuable experience in chemical engineering processes, pharmaceutical production technology, regulatory compliance, and industrial plant operations. Early‑career exposure to pharmaceutical manufacturing allows professionals to develop technical skills that are highly valued across pharmaceutical companies, chemical manufacturers, and contract manufacturing organizations. Career progression opportunities may include: • API Production Officer • Chemical Process Engineer • Pharmaceutical Manufacturing Executive • Quality Assurance Specialist • Pharmaceutical Plant Operations Manager Because the pharmaceutical industry continues to expand globally, professionals trained in API manufacturing and chemical production systems remain in strong demand. Frequently Asked Questions (FAQs) Who can apply for the Global Calcium API Production fresher role? Candidates who completed Diploma Chemical Engineering, BSc Chemistry, or BTech Chemical Engineering in 2024 or 2025 can apply. Is prior pharmaceutical experience required? No. This position is designed for fresh graduates who want to start their careers in API production. Where is the job location? The role is based at Global Calcium’s manufacturing units located in SIPCOT Phase I, Hosur. What skills are required for API production roles? Candidates should have a basic understanding of chemical processes, manufacturing safety practices, and interest in pharmaceutical production systems. How can candidates apply? Interested applicants can send their updated resume to the official HR email address mentioned in the job announcement. Job Summary Company Global Calcium Pvt. Ltd. Vacancies API Production Trainee Required Education Diploma Chemical Engineering, BSc Chemistry, BTech Chemical Engineering Experience Freshers (2024 & 2025 Passouts) [...] Read more...

Malladi walk-in Production, QA, QC

Mehta walk‑in R&D, QA, Production

Clinical Database Programmer Role for Freshers Oryxion

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now CRO Hiring Alert: Clinical Database Programmer Role for Freshers The clinical research industry continues to expand rapidly, creating new opportunities for professionals skilled in clinical data systems and electronic data capture platforms. Oryxion has announced hiring for the position of Clinical Database Programmer in Bengaluru, opening a promising opportunity for candidates interested in clinical data management and global clinical trial technology. For pharmacy, life science, and technology graduates aiming to enter the clinical research organization (CRO) sector, this role offers direct exposure to clinical database development used in international clinical trials. Early‑career professionals will gain hands‑on experience designing clinical study databases and supporting global pharmaceutical research programs. As pharmaceutical companies increasingly rely on digital clinical trial platforms, skilled professionals who understand clinical database programming and data quality standards are becoming highly valuable in the drug development ecosystem. Company Overview Oryxion is a clinical research and healthcare technology organization supporting pharmaceutical companies and global clinical trial teams. The company specializes in clinical data management, database programming, clinical trial analytics, and regulatory compliant data systems used across global drug development programs. Through advanced electronic data capture (EDC) technologies, Oryxion helps research organizations manage large volumes of clinical trial data while ensuring regulatory compliance and high data quality standards. Clinical database programming teams at Oryxion collaborate with clinical data managers, statisticians, and research teams to build secure, compliant databases that capture patient data during clinical trials. These databases ultimately support statistical analysis, regulatory submissions, and drug approval decisions by global health authorities. Career Outlook for Clinical Data & Safety Science Professionals in 2026 The demand for professionals skilled in clinical data science, clinical database programming, and healthcare analytics is expected to grow significantly by 2026. Pharmaceutical companies and CRO organizations are investing heavily in digital clinical trial infrastructure to improve data accuracy and accelerate regulatory submissions. Clinical database programmers play a critical role in building and maintaining the electronic systems that collect clinical trial data from research sites worldwide. Their work ensures that patient data is captured accurately and complies with global regulatory requirements. Professionals who begin their careers in clinical database programming often advance into roles such as Clinical Data Manager, Clinical Data Scientist, EDC Specialist, Clinical Systems Analyst, or Healthcare Data Engineer. With increasing adoption of electronic data capture systems and clinical data standards, the field offers strong long‑term career prospects. Job Role & Responsibilities The Clinical Database Programmer will support the design, development, and maintenance of clinical trial databases used in global clinical studies. Key responsibilities include: Design and develop clinical study databases within electronic data capture systems Configure electronic case report forms (eCRFs) according to study protocols and data management plans Develop edit checks and validation rules to ensure accurate clinical data capture Configure database logic, field properties, and form structures within the EDC system Perform user acceptance testing (UAT) and database validation activities Identify and resolve data discrepancies during database testing and live clinical trials Review study protocols and clinical documentation to support accurate database configuration Maintain documentation related to database build specifications and testing procedures Support database freeze and database lock activities before statistical analysis Follow standard operating procedures (SOPs) and regulatory compliance guidelines The role requires close collaboration with clinical data managers, biostatisticians, statistical programmers, and clinical operations teams to ensure clinical data accuracy and reliability. Eligibility / Qualifications Candidates interested in this clinical research opportunity should meet the following qualifications: Degree in Life Sciences, Pharmacy, Computer Science, Statistics, or related discipline Interest in clinical data management, database programming, and clinical trial systems Understanding of clinical trial data structures and electronic data capture platforms Strong analytical thinking and attention to detail Ability to collaborate with multidisciplinary clinical research teams Relevant education backgrounds may include: B.Pharm, M.Pharm, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Tech Computer Science, B.Sc Statistics, M.Sc Bioinformatics, M.Sc Data Science, BCA, MCA. Experience Requirements Oryxion is looking for early career professionals with knowledge of clinical database programming or clinical data management. 0 to 2 years of experience in clinical database programming or clinical data management Experience working with electronic data capture platforms is preferred Understanding of clinical trial data standards and CRF design Candidates who have completed internships or training in clinical data management or EDC programming may also be considered. Technical Skills Applicants should be familiar with clinical data systems used in global clinical trials, including: Medidata Rave Oracle Clinical Veeva EDC Inform EDC or similar clinical data platforms Knowledge of CDISC data standards and clinical trial database validation processes will be considered an advantage. Location & Salary Location: Bengaluru, Karnataka, India Application Process Interested candidates can apply through the official application link provided by Oryxion. Apply here: https://forms.office.com/pages/responsepage.aspx?id=Fw13o2lYkEut8iyPgxnhQ-LlqKLzmghLkqPuB-hPmERUNjIwUUJYWVdCNUpGODNNSTZESTlQNFI3Ui4u&route=shorturl Applicants should prepare an updated resume highlighting experience with clinical data systems, database programming knowledge, and any exposure to clinical research projects. Early applications are recommended as positions may be filled quickly in fast‑growing CRO organizations. Frequently Asked Questions Who can apply for the Oryxion Clinical Database Programmer role? Candidates from life science, pharmacy, computer science, or statistics backgrounds with interest in clinical data management can apply. Is prior experience required for this role? Candidates with 0–2 years of experience in clinical database programming or clinical data management are eligible. Which EDC systems are useful for this role? Knowledge of platforms such as Medidata Rave, Oracle Clinical, Inform, or Veeva EDC is beneficial. What career growth opportunities exist in clinical database programming? Professionals can progress into roles such as Clinical Data Manager, EDC Specialist, Clinical Data Scientist, or Clinical Systems Analyst. Summary Category Details Company Oryxion Vacancies Clinical Database Programmer Required Education B.Pharm, M.Pharm, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Tech Computer Science, M.Sc Bioinformatics Experience 0–2 years in clinical database programming or clinical data management Location Bengaluru, Karnataka Department Clinical Data Management / Database Programming [...] Read more...

Fortrea Opens Regulatory Operations Role for Pharma Freshers

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Fortrea Hiring Regulatory Operations Assistant I for Pharma Graduates Global clinical research organization Fortrea has announced hiring for the position of Regulatory Operations Assistant I in Mumbai, creating a valuable opportunity for B.Pharm and life science graduates who want to enter the regulatory affairs and drug development sector. For many pharmacy graduates, breaking into global regulatory operations can be challenging. This Fortrea opening provides early‑career professionals the chance to work on regulatory documentation submitted to major global health authorities including the US FDA, European Medicines Agency, Japan PMDA, and other international regulatory agencies. With pharmaceutical companies expanding global drug approvals and clinical development programs, professionals trained in regulatory operations and compliance are becoming essential to the healthcare industry. Company Overview Fortrea is a global contract research organization (CRO) focused on clinical development, regulatory services, and drug lifecycle support for pharmaceutical and biotechnology companies. The company provides scientific expertise across clinical trials, regulatory strategy, pharmacovigilance, and data management. Operating in multiple countries, Fortrea supports pharmaceutical sponsors in bringing innovative therapies to market while ensuring compliance with international regulatory guidelines. The organization works closely with global health authorities and industry partners to accelerate drug development and maintain high standards of quality and patient safety. Fortrea is known for its strong regulatory science capabilities and its ability to help pharmaceutical companies prepare documentation, submissions, and compliance reports required for drug approvals in regulated markets. Career Outlook for Safety Science & Regulatory Analysts in 2026 The pharmaceutical regulatory landscape is evolving rapidly as companies expand global clinical trials and introduce new therapies across regulated markets. By 2026, demand for professionals specializing in regulatory operations, pharmacovigilance, and safety science analytics is expected to increase significantly. Regulatory operations analysts play a critical role in compiling drug development documentation, managing regulatory submissions, and ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and International Council for Harmonisation (ICH) guidelines. Professionals who start their careers in regulatory operations often progress into roles such as Regulatory Affairs Specialist, Global Submission Manager, Drug Safety Associate, or Regulatory Strategy Lead. Experience with electronic regulatory submission systems and global regulatory frameworks can open doors across pharmaceutical companies, CROs, and biotechnology firms. Job Role & Responsibilities The Regulatory Operations Assistant I will support preparation, compilation, and management of regulatory documentation required for global drug submissions. Key responsibilities include: Create, review, and compile regulatory specifications and documentation for submission to international health authorities Support regulatory submissions to agencies such as the US FDA, European Medicines Agency (EMA), Japan PMDA, and other global authorities Ensure compliance with Good Laboratory Practice (GLP), Good Documentation Practice (GDP), and current Good Manufacturing Practices (cGMP) Perform analytical testing including assay, related substances, dissolution, and content uniformity Support validation activities such as cleaning validation and process validation Maintain regulatory and training documentation according to company and client requirements Operate laboratory and analytical instruments including HPLC, UPLC, GC, Karl Fischer, dissolution testers, particle size analyzers, and analytical balances Assist in onboarding, training, and mentoring new associates within regulatory operations teams Perform tasks assigned by department leadership and support regulatory project requirements The role requires attention to detail, documentation accuracy, and strong collaboration with quality assurance, analytical science, and regulatory teams. Eligibility / Qualifications Candidates interested in this regulatory operations opportunity should meet the following qualifications: Bachelor’s degree in Pharmacy or related life science discipline Advanced degrees such as M.Pharm, MSc, or PhD may also be considered Knowledge of pharmaceutical product lifecycle and regulatory compliance standards Familiarity with GxP, ICH guidelines, and regulatory submission processes is desirable Strong analytical and documentation skills Ability to manage multiple tasks and maintain regulatory accuracy Relevant education backgrounds include: B.Pharm, M.Pharm, MSc Pharmaceutical Chemistry, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, Pharmaceutics, Pharmaceutical Analysis, Regulatory Affairs. Experience Fortrea is seeking candidates with early career experience in pharmaceutical regulatory or quality environments. 0 to 3 years of experience in regulatory affairs, quality assurance, analytical science, pharmaceutics, or drug development Knowledge of regulatory documentation systems or electronic regulatory information management systems is an advantage Technical proficiency in Microsoft Office and documentation tools Candidates with certifications or diplomas in regulatory affairs may receive additional consideration. Location & Salary Location: Mumbai, India Salary: Competitive compensation based on experience and role responsibilities. Global CRO organizations typically provide structured salary packages, performance incentives, and long‑term career development opportunities. Application Process Interested candidates can apply through the official Fortrea careers portal using the link below. Apply here: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Mumbai/Regulatory-Operations-Assistant-I_26654 Applicants should prepare an updated resume highlighting regulatory knowledge, analytical laboratory skills, and familiarity with pharmaceutical compliance guidelines. Due to application deadlines, candidates are encouraged to apply as soon as possible. Frequently Asked Questions Who can apply for the Fortrea Regulatory Operations Assistant role? Pharmacy graduates and life science candidates with knowledge of pharmaceutical regulatory processes can apply. Is this role suitable for freshers? Yes. Candidates with 0–3 years of experience in regulatory affairs, quality assurance, or pharmaceutical analytical roles are eligible. What skills are important for regulatory operations careers? Knowledge of pharmaceutical regulations, documentation accuracy, analytical testing methods, and regulatory submission processes are important skills. What career growth opportunities exist in regulatory operations? Professionals can progress into Regulatory Affairs Specialist, Global Regulatory Manager, Drug Safety Associate, or Regulatory Strategy roles within pharmaceutical companies and CRO organizations. Summary Category Details Company Fortrea Vacancies Regulatory Operations Assistant I Required Education B.Pharm, M.Pharm, MSc Pharmaceutical Chemistry, MSc Biotechnology, MSc Microbiology, MSc Biochemistry Experience 0–3 years in regulatory affairs, QA, analytical science or pharmaceutics Location Mumbai Department Regulatory Operations [...] Read more...

BioMatrix Walk‑In QC QA

IIT Hyderabad SURE 2026: 250 Research Internship Seats for Students

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now IIT Hyderabad Announces SURE 2026 Research Internship with ₹15,000 Fellowship Students aiming to build strong research careers in science, technology, and innovation now have a major opportunity. The Indian Institute of Technology Hyderabad (IIT Hyderabad) has officially announced applications for the Summer Undergraduate Research Exposure (SURE) Internship 2026, offering hands‑on research experience along with a fellowship of up to ₹15,000. The internship is designed for high‑performing students from universities across India who want early exposure to advanced scientific research. Selected candidates will work directly with IIT Hyderabad faculty mentors and research groups during the summer research program. For students from life sciences, chemistry, physics, biotechnology, engineering, and design disciplines, the SURE internship offers a valuable entry into academic research, scientific innovation, and future postgraduate research opportunities. Company Overview The Indian Institute of Technology Hyderabad (IIT Hyderabad) is one of India’s premier institutions for engineering, science, and technology education. Known for its strong research ecosystem, the institute actively promotes innovation, interdisciplinary collaboration, and advanced scientific discovery. IIT Hyderabad has built a reputation for cutting‑edge research across fields such as biotechnology, artificial intelligence, materials science, chemistry, physics, and biomedical engineering. Through programs like the SURE Internship, the institute encourages undergraduate and postgraduate students to participate in meaningful research projects. By offering mentorship under experienced faculty and access to world‑class laboratories, the program helps students develop research skills that are essential for careers in academia, pharmaceuticals, biotechnology, and technology innovation sectors. Career Outlook for Research & Scientific Analysts in 2026 Scientific research careers are expanding rapidly as industries invest heavily in biotechnology, pharmaceuticals, artificial intelligence, and advanced materials. By 2026, organizations across healthcare, life sciences, and technology sectors are expected to demand professionals with strong research and analytical skills. Internship programs such as SURE help students build early research exposure, which is highly valuable for careers in pharmaceutical research, biotechnology innovation, clinical research, and scientific data analysis. Students who participate in research internships often gain an advantage when applying for higher studies, research fellowships, or industry R&D positions. Hands‑on research experience also strengthens skills in scientific problem solving, laboratory techniques, data interpretation, and academic collaboration. These competencies are essential for future careers in research laboratories, biotech startups, pharmaceutical companies, and advanced technology organizations. Internship Program Details The Summer Undergraduate Research Exposure (SURE) Internship provides students the opportunity to work closely with IIT Hyderabad faculty mentors on active research projects. Program highlights include: Exposure to real research projects in science and engineering Mentorship from IIT Hyderabad faculty members Hands‑on laboratory and research experience Opportunity to develop research methodology and analytical skills Academic exposure to interdisciplinary research environments This program allows students to experience the daily workflow of research labs and understand how scientific discoveries are developed and tested. Eligibility / Qualifications Candidates interested in the SURE Internship must meet the following criteria: Applicants must NOT be students of IIT Hyderabad Must be full‑time students during the application period and until internship completion Should belong to one of the following academic categories: Eligible students include: First Year M.Sc students in Mathematics, Physics, Chemistry, or Biology First Year M.A students Second or Third Year B.Tech or B.Des students (all branches) Third or Fourth Year Integrated B.Tech‑M.Tech students Applicants must be among the top 20% of their class based on CGPA or percentage in previous academic years. Certification from the Head of Institution or Principal is required during the application process. Students must be available for full‑time participation during the internship period. Part‑time or online internships are not permitted. Relevant academic programs include: M.Sc Chemistry, M.Sc Physics, M.Sc Mathematics, M.Sc Biology, B.Tech Biotechnology, B.Tech Chemical Engineering, B.Tech Computer Science, B.Tech Mechanical Engineering, B.Des, Integrated B.Tech‑M.Tech programs and other related disciplines. Fellowship, Duration & Facilities Selected interns will receive financial support during the program. Fellowship options: ₹7,500 for one month ₹10,000 for one and a half months ₹15,000 for the full two‑month internship Interns may choose the duration between one month and two months depending on their availability. Tentative internship period: 15 May 2026 to 14 July 2026 Accommodation: Hostel accommodation will be provided in IIT Hyderabad student hostels Mess charges must be paid by the interns Application Process Students must apply through the official IIT Hyderabad online portal. Offline applications or email submissions will not be accepted. Important dates: Announcement of applications: 28 February 2026 Last date to submit online application: 10 March 2026 Result announcement: 15 April 2026 (Tentative) Internship start date: 15 May 2026 (Tentative) Apply through the official website: https://www.iith.ac.in/news/2026/02/27/Summer-Undergraduate-Research-Exposure/ Additional details: https://iith.ac.in/research/SURE/ Applicants are advised to complete their application before the deadline because late submissions will not be accepted. Selection Procedure The selection process includes multiple evaluation stages: Initial screening of applications Academic performance evaluation Assessment of extracurricular research or academic achievements Online interview conducted by the respective department or faculty mentor Selection may also consider achievements in national competitions, Olympiads, National Talent Search examinations, or research activities performed during academic studies. Final results will be announced on the SRC office webpage of IIT Hyderabad. Frequently Asked Questions Who can apply for the IIT Hyderabad SURE Internship? Students from universities across India who meet the eligibility criteria and are not studying at IIT Hyderabad can apply. Is this internship paid? Yes. Selected interns receive a fellowship of up to ₹15,000 depending on the duration of the internship. Is accommodation available? Yes. Hostel accommodation is provided at IIT Hyderabad. However, interns must pay their own mess charges. Is online participation allowed? No. The internship requires full‑time physical participation at the IIT Hyderabad campus. Summary Category Details Organization IIT Hyderabad Program Summer Undergraduate Research Exposure (SURE) Internship 2026 Vacancies 250 Interns (100 seats reserved for girls) Required Education M.Sc (Maths, Physics, Chemistry, Biology), MA First Year, B.Tech, B.Des, Integrated B.Tech‑M.Tech Experience Students in Top 20% of their academic program Fellowship Up to ₹15,000 for 2 months Location IIT Hyderabad Campus Duration 1 to 2 months between May and July 2026 [...] Read more...

Certified HCC Medical Coders – Freshers SpyHealth Hiring | Hyderabad

Omega Healthcare Hiring Trainee Medical Coders | ED, Home Health

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Medical Coding Fresher Hiring: Pharma Graduates Can Enter Healthcare IT Fresh graduates from pharmacy and life science backgrounds now have a new entry point into the rapidly expanding healthcare data industry. Omega Healthcare has announced freshers hiring for the role of Trainee Medical Coder at its Trichy location, opening opportunities for B.Pharm, M.Pharm, Pharm.D and life science graduates. For many pharmacy graduates exploring non-clinical careers, medical coding has become one of the fastest growing options in healthcare analytics and revenue cycle management. This recruitment provides structured training followed by a full-time role in a global healthcare outsourcing company. Company Overview Omega Healthcare is a global healthcare outsourcing organization that provides technology-enabled solutions for hospitals, healthcare providers, and insurance companies. The company specializes in medical coding, healthcare analytics, revenue cycle management, and clinical documentation services. With delivery centers across India and global operations supporting major healthcare systems, Omega Healthcare plays a key role in improving clinical documentation accuracy and healthcare data management. The organization employs thousands of healthcare professionals working across coding, billing, clinical data processing, and healthcare analytics functions. The company focuses on developing healthcare domain talent through structured training programs that help fresh graduates build careers in medical coding, healthcare data analysis, and revenue cycle operations. Career Outlook for Medical Coding & Healthcare Data Professionals in 2026 The demand for certified medical coders and healthcare documentation specialists continues to grow as hospitals digitize medical records and insurance processing systems. By 2026, healthcare providers worldwide are expected to rely heavily on skilled professionals who can translate clinical documentation into standardized medical codes. Medical coding professionals play an essential role in healthcare reimbursement systems, insurance claim processing, and clinical data analysis. Their work ensures that hospitals maintain accurate medical documentation while complying with international healthcare regulations. Graduates who begin their careers as trainee medical coders can later specialize in areas such as inpatient coding, emergency department coding, clinical documentation improvement, or healthcare analytics. Career progression may include roles such as Senior Medical Coder, Coding Auditor, Clinical Data Analyst, or Healthcare Revenue Cycle Specialist. Job Role & Responsibilities The Trainee Medical Coder role involves converting clinical diagnoses, procedures, and medical documentation into standardized medical codes used for healthcare billing and analysis. Key responsibilities include: Review patient medical records and clinical documentation Assign accurate medical codes based on diagnoses and procedures Maintain coding accuracy according to healthcare coding standards Ensure proper documentation for insurance claims and reimbursement processes Collaborate with healthcare teams to clarify clinical information Maintain confidentiality and compliance with healthcare data regulations Selected candidates will undergo structured training before beginning coding assignments. Eligibility / Qualifications Candidates interested in this healthcare career opportunity should meet the following criteria: Degree in Pharmacy, Life Sciences, or Paramedical disciplines Strong knowledge of Human Anatomy, Physiology, and Medical Terminology Good analytical and documentation skills Willingness to undergo training in medical coding practices Relevant education backgrounds may include: B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Nursing, BPT, BMLT and other Paramedical courses. Both certified and non-certified candidates are eligible to apply. Training & Certification Omega Healthcare provides structured training for selected candidates to prepare them for professional medical coding roles. Training details include: Medical Coding Training for approximately 55–65 working days Training period does not include salary or stipend Candidates will receive role-specific coding exposure during training Department allocation will be based on interview performance. For Home Health department: BCHH-C certification will be provided. For Emergency Department (ED): CPC certification may be provided after onboarding based on employee performance. Location & Salary Location: Trichy, Tamil Nadu Salary: Approximately ₹19,000 per month after successful completion of training and interview evaluation. Healthcare outsourcing companies often provide structured career paths and opportunities to obtain globally recognized coding certifications. Application Process Interested candidates can apply by sending their resume to the official recruitment email below. Email Application: Mubaraknisha.Meeranmydeen@omegahms.com Applicants should include updated academic details and highlight knowledge of anatomy, physiology, and medical terminology. Due to limited training seats, early application is recommended. Frequently Asked Questions Who can apply for Omega Healthcare medical coding roles? Pharmacy graduates, life science graduates, and paramedical degree holders can apply. Is prior medical coding certification required? No. Both certified and non-certified candidates are eligible for this trainee role. Is training provided for freshers? Yes. Omega Healthcare provides structured medical coding training for 55–65 working days. What certifications may be offered during the role? Candidates may receive BCHH-C certification for Home Health coding or CPC certification based on performance in the Emergency Department coding team. Summary Category Details Company Omega Healthcare Vacancies Trainee Medical Coder Required Education B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, BPT, BMLT, Paramedical Courses Experience Freshers Eligible Location Trichy, Tamil Nadu Salary ₹19,000 per month after training Department Emergency Department Coding, Home Health Coding [...] Read more...

Apollo Hospitals Hiring Pharmacist – Supply Chain Management Role

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Apollo Hospitals Opens Pharmacist Supply Chain Roles for Pharma Graduates Pharmacy and healthcare graduates looking to enter the hospital supply chain and clinical pharmacy ecosystem now have a strong opportunity at Apollo Hospitals. The healthcare giant has announced recruitment for the role of Pharmacist – Supply Chain Management in Chennai, offering pharmacy graduates the chance to work inside one of India’s most respected hospital networks. For B.Pharm and other life science graduates aiming to build careers in hospital pharmacy operations, drug distribution systems, and healthcare logistics, this hiring comes at an important time. As hospitals expand digital pharmacy operations and medicine distribution networks, supply chain pharmacists are becoming critical to safe and efficient patient care. Company Overview Apollo Hospitals is one of India’s most recognized healthcare institutions and a pioneer in modern hospital services. Over the past several decades, the organization has built a reputation for advanced medical technology, specialized treatments, and high standards of patient‑centric healthcare delivery. The hospital group operates a vast network of hospitals, pharmacies, diagnostic centers, and telemedicine platforms across India. Through innovation, research initiatives, and continuous investment in healthcare infrastructure, Apollo Hospitals continues to shape the future of healthcare delivery in the country. Beyond clinical excellence, the organization is also known for developing strong hospital pharmacy systems, medication safety protocols, and digital healthcare supply chains. This makes it an attractive workplace for pharmacy professionals interested in hospital operations and pharmaceutical supply management. Career Outlook for Healthcare Supply Chain & Safety Professionals in 2026 Healthcare supply chains are evolving rapidly as hospitals adopt digital inventory systems, automated pharmacy dispensing, and integrated drug safety monitoring platforms. By 2026, the demand for pharmacists working in supply chain management, medication safety, and hospital logistics is expected to grow significantly. Professionals working in pharmacy supply chains help ensure the availability, quality, and traceability of medicines across hospital departments. Their work directly impacts patient safety, treatment efficiency, and regulatory compliance. For pharmacy graduates, starting in hospital supply chain roles provides strong exposure to pharmaceutical inventory management, healthcare operations, and medication distribution systems. Over time, professionals can advance into roles such as Pharmacy Operations Manager, Hospital Supply Chain Specialist, or Healthcare Logistics Consultant. Job Role & Responsibilities The Pharmacist – Supply Chain Management role focuses on managing medicine inventory, ensuring proper drug storage, and supporting efficient pharmaceutical supply across hospital departments. Key responsibilities include: Manage hospital pharmacy inventory and medication supply systems Ensure accurate procurement, storage, and distribution of pharmaceutical products Maintain drug inventory records and support supply chain documentation Coordinate with pharmacy teams, procurement teams, and healthcare professionals Monitor stock levels and prevent medicine shortages within hospital units Ensure medicines are handled according to safety and regulatory guidelines Support medication safety initiatives and quality compliance programs The role plays a crucial part in maintaining uninterrupted medicine availability for patient care while supporting hospital operational efficiency. Eligibility / Qualifications Candidates interested in this healthcare pharmacy opportunity should meet the following criteria: Graduate degree in Pharmacy or relevant life science discipline Strong understanding of hospital pharmacy practices and pharmaceutical products Good communication and teamwork skills Ability to work in fast‑paced healthcare environments Basic understanding of inventory management and pharmaceutical supply processes Relevant education backgrounds may include: B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry. Location & Salary Location: Chennai, Tamil Nadu, India Salary: Competitive hospital pharmacy salary packages based on experience and role responsibilities. Leading healthcare organizations typically offer structured compensation along with career development opportunities in pharmacy management. Application Process Interested candidates can apply online through the official Apollo Hospitals career portal. Apply here: https://cgs.fa.ap2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2/job/39071 Applicants should submit an updated resume highlighting pharmacy education, hospital training exposure, and any relevant experience in pharmacy operations or healthcare supply chain roles. Frequently Asked Questions Who can apply for the Apollo Hospitals Pharmacist role? Candidates with a pharmacy degree such as B.Pharm or M.Pharm and relevant healthcare knowledge can apply. Is this role suitable for freshers? Yes. Pharmacy graduates looking to start careers in hospital pharmacy operations or pharmaceutical supply chain management can apply. What does a supply chain pharmacist do in hospitals? A supply chain pharmacist manages medicine inventory, ensures proper drug storage, coordinates with procurement teams, and maintains medication availability across hospital departments. What career growth options exist in hospital pharmacy supply chain roles? Professionals can grow into Pharmacy Supervisor, Pharmacy Operations Manager, Hospital Supply Chain Manager, or Healthcare Procurement Specialist roles. Summary Category Details Company Apollo Hospitals Vacancies Pharmacist – Supply Chain Management Required Education B.Pharm, M.Pharm, Pharm.D, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry Experience Freshers and experienced pharmacy professionals may apply Location Chennai, Tamil Nadu Job Type Hospital Pharmacy / Healthcare Supply Chain [...] Read more...

ICON Hiring Junior Statistician / Biostatistician I – Clinical Research Opportunity

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now ICON Hiring Junior Statistician / Biostatistician I – Clinical Research Opportunity Clinical research hiring is gaining momentum in India, and ICON plc has opened a Junior Statistician (Biostatistician I) opportunity for candidates interested in clinical trials and healthcare data science. For graduates in statistics, biostatistics, pharmacy, biotechnology, and related life science fields, this role offers a direct entry into the global clinical research industry. This hiring comes at a time when pharmaceutical companies and CROs are investing heavily in data-driven clinical development. Early‑career professionals with statistical analysis skills and knowledge of clinical trials methodology can gain valuable exposure to global drug development programs. Company Overview ICON plc is a global healthcare intelligence and clinical research organization known for supporting pharmaceutical, biotechnology, and medical device companies in drug development and clinical trials. The company works with sponsors worldwide to deliver high‑quality clinical research services and data analytics solutions. With operations across multiple countries, ICON has built a strong reputation in clinical trial management, regulatory support, pharmacovigilance, and biostatistics. The organization focuses on advancing healthcare innovation through data science, real‑world evidence, and precision medicine. Career Outlook for Safety Science & Biostatistics Analysts in 2026 The demand for biostatisticians and safety science analysts is expanding rapidly across the pharmaceutical and clinical research industry. By 2026, CROs and drug manufacturers are expected to rely heavily on advanced analytics, statistical modeling, and regulatory‑grade data interpretation. Professionals skilled in statistical programming, clinical data analysis, and real‑world evidence generation will play a key role in evaluating drug safety, treatment outcomes, and trial results. Entry‑level roles like Junior Statistician provide a strong foundation for long‑term careers in clinical research, regulatory science, and healthcare data analytics. Job Role & Responsibilities As a Biostatistician I at ICON, the selected candidate will contribute to statistical planning and analysis for clinical trials and research studies. Key responsibilities include: Assist in the design and development of case report forms with statistical considerations Review clinical study databases, edit checks, and coding conventions to maintain data integrity Develop statistical analysis plans for assigned clinical studies Create statistical tables, figures, and listings for clinical study reports Perform statistical analysis to interpret research data and generate insights Support preparation of integrated study reports and statistical methods documentation Collaborate with biostatistics teams, clinical programmers, and research scientists Eligibility / Qualifications Candidates interested in this clinical research career opportunity should meet the following qualifications: Master’s degree in Statistics, Biostatistics, Mathematics, Data Science, or related analytical discipline Hands‑on experience with R programming for statistical analysis Minimum 1 year of experience in statistics, biostatistics, or pharmaceutical research environment Strong understanding of clinical trial design and statistical methodology Familiarity with statistical software packages such as SAS Knowledge of regulatory standards and clinical research data management practices Good communication and technical documentation skills Relevant education backgrounds may include: M.Sc Statistics, M.Sc Biostatistics, M.Sc Mathematics, M.Sc Data Science, M.Pharm, B.Pharm, M.Sc Biotechnology, M.Sc Bioinformatics, M.Sc Computational Biology. Location & Salary Location: Bangalore, Chennai, Bengaluru (Hybrid or Remote options may be available depending on the team). Salary: Competitive salary package based on experience and role level. Global CRO companies typically offer attractive compensation along with performance‑based incentives and career growth opportunities. Benefits ICON offers a wide range of employee benefits designed to support professional growth and personal well‑being: Competitive salary and performance incentives Health insurance coverage for employees and family Retirement planning benefits Global employee assistance program Flexible work‑life balance policies Professional development and learning opportunities Application Process Interested candidates can apply online through the official ICON careers portal. Apply here: https://careers.iconplc.com/job/junior-statistician-in-india-bangalore-jid-48895 Applicants should prepare an updated resume highlighting statistical programming experience, academic background, and any exposure to clinical trial data analysis. Frequently Asked Questions Who can apply for the ICON Junior Statistician role? Candidates with a Master’s degree in Statistics, Biostatistics, Mathematics, Data Science, Pharmacy, or related life science fields with statistical programming knowledge can apply. Is prior experience required? Yes. ICON prefers candidates with at least one year of experience in statistics, biostatistics, or pharmaceutical research. What skills are important for this role? Strong statistical analysis knowledge, R or SAS programming skills, understanding of clinical trials methodology, and the ability to interpret healthcare data are important. Is the role suitable for freshers? Fresh graduates with strong statistical programming knowledge and internship exposure in clinical research may still consider applying. Summary Category Details Company ICON plc Vacancies Junior Statistician, Biostatistician I Required Education M.Sc Statistics, M.Sc Biostatistics, M.Sc Mathematics, M.Sc Data Science, M.Pharm, B.Pharm, M.Sc Biotechnology, M.Sc Bioinformatics Experience Minimum 1 year in statistics, biostatistics, or pharmaceutical research Location Bangalore, Chennai, Bengaluru Job Type Clinical Research / Biostatistics [...] Read more...

Newest | Active | Popular

Neeta Katgi

active 21 hours ago
Sudheer Vanguri

active 21 hours ago
Balu p

active a day ago
RANDHIR SINGH

active a day ago
Gokulraj

active a day ago

See all