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Abryl Laboratories Hiring B Pharm Professionals | QA & Production Openings | Dera Bassi

Walk-in opportunities at Abryl Laboratories for QA & Production roles. B Pharm graduates with 2–6 years experience at Dera Bassi.

Abryl Laboratories Pvt. Ltd., a USFDA-approved injectable manufacturing plant, is inviting skilled and qualified professionals for its Production and Quality Assurance departments. This is a golden opportunity for B Pharm graduates with experience in sterile or injectable plant operations to advance their pharmaceutical careers with one of India’s rapidly growing regulated facilities.

Apply now and become part of an innovative organization that values technical excellence and quality-driven pharmaceutical manufacturing.

Company Overview

Abryl Laboratories Pvt. Ltd., located in Dera Bassi, Punjab, is a leading injectable manufacturing company accredited by USFDA and other major regulatory authorities. Known for its commitment to sterility assurance, cGMP compliance, and innovation, Abryl Laboratories specializes in the development and production of high-quality injectable formulations for global markets.

With a strong focus on research, manufacturing excellence, and regulatory compliance, Abryl ensures the highest standards in product safety and therapeutic efficacy.

Job Role & Responsibilities

Abryl Laboratories is hiring for the following departments:

1. Production Department – QMS Section

Position: Executive / Officer
Experience: 2–6 years
Qualification: B Pharm
Key Responsibilities:

  • Manage and maintain Quality Management Systems (QMS) within the production environment
  • Ensure adherence to GMP and regulatory guidelines
  • Coordinate deviation control, CAPA, and change control processes
  • Monitor and ensure compliance with Batch Manufacturing Records (BMR) and documentation standards
  • Support validation, qualification, and risk assessment activities

2. Quality Assurance (QA) Department – IPQA Section (Female Candidates Preferred)

Position: Executive / Officer
Experience: 2–4 years
Qualification: B Pharm
Key Responsibilities:

  • Conduct In-Process Quality Assurance (IPQA) checks in sterile manufacturing areas
  • Perform line clearance and process validation
  • Ensure compliance with sterility assurance protocols and documentation accuracy
  • Review production and packing activities for adherence to quality standards
  • Collaborate with production teams to ensure continuous quality improvement

Note: Candidates must have relevant experience in an injectable manufacturing facility.

Eligibility / Qualifications

  • Required Education: B Pharm (Bachelor of Pharmacy)
  • Preferred Courses: Pharmaceutical Technology, Industrial Pharmacy, Pharmaceutical Quality Assurance, Drug Regulatory Affairs
  • Experience Required: 2–6 years in sterile/injectable manufacturing setup
  • Core Skills: GMP Documentation, QMS, IPQA, Process Validation, Deviation Handling, CAPA Implementation, Regulatory Compliance

Location & Salary

  • Location: Dera Bassi, Punjab
  • Salary: Competitive and commensurate with experience

Abryl Laboratories offers a performance-driven work culture, continuous learning environment, and the opportunity to work with world-class manufacturing technologies.

Application Process

Interested candidates can apply immediately by sharing their updated resume and relevant documents.

Email: hr.2@abryl.in
WhatsApp: +91 9882859675

Apply before 15 October 2025 to secure your interview slot!

Candidates are encouraged to highlight relevant experience in sterile/injectable manufacturing in their applications.

Why Join Abryl Laboratories?

  • Opportunity to work in a USFDA-approved plant with advanced injectable technology
  • Exposure to global pharmaceutical manufacturing standards
  • Supportive team culture and growth-oriented environment
  • Direct involvement in quality and compliance functions impacting patient safety

FAQs

1. Who is eligible to apply?
B Pharm graduates with 2–6 years of relevant injectable plant experience are eligible.

2. What departments are currently hiring?
Abryl Laboratories is hiring for Production (QMS) and Quality Assurance (IPQA) roles.

3. Are female candidates encouraged to apply?
Yes, female candidates are especially encouraged for the QA-IPQA positions.

4. Where is the job location?
The openings are based at Dera Bassi, Punjab, in a USFDA-approved injectable facility.

5. How can I apply?
Send your resume to hr.2@abryl.in or WhatsApp at +91 9882859675.

Apply Now

Don’t miss your chance to join a global pharmaceutical leader.
Apply now and take your career to the next level with Abryl Laboratories’ state-of-the-art injectable manufacturing facility.

Last Date to Apply: 15 October 2025
Location: Dera Bassi, Punjab

Apply before the deadline to secure your spot in the selection process!

Abryl Laboratories Job Summary Table

CategoryDetails
CompanyAbryl Laboratories Pvt. Ltd. (USFDA Approved)
VacanciesProduction (QMS), QA (IPQA)
Required EducationB Pharm
Experience2–6 Years
Preferred GenderFemale (QA-IPQA)
LocationDera Bassi, Punjab
Contact Emailhr.2@abryl.in
WhatsApp Contact+91 9882859675
Apply Before15 October 2025

MBA, B Pharm, ITI Openings – Strava Healthcare Walk-In | Ahmedabad

Apply for HR, Accounts & Production vacancies at Strava Healthcare Walk-in Drive, Ahmedabad. Openings for MBA, B Pharm, ITI freshers & experienced.

Strava Healthcare Pvt. Ltd. is inviting talented professionals and freshers to join its expanding team. With multiple vacancies across HR, Accounts, and Production departments, this walk-in drive is an excellent opportunity for candidates seeking growth in the pharmaceutical sector. The recruitment drive will be held on 5th October 2025 from 9:00 AM to 4:00 PM at the company premises in Ahmedabad.

Company Overview

Strava Healthcare Private Limited is a trusted name in the pharmaceutical industry, specializing in the production of high-quality medicines. Known for innovation and strict adherence to global compliance standards, Strava offers a supportive workplace where employees are encouraged to build meaningful careers. With advanced manufacturing facilities and a strong focus on research, Strava is contributing to affordable healthcare solutions across India.

Job Role & Responsibilities

1. HR Department

  • Position: Trainee Officer
  • Openings: 1
  • Qualification: MBA, BBA, M.Com, B.Com
  • Experience: Fresher
  • Responsibilities: Support HR operations, recruitment, onboarding, employee engagement, and documentation.

2. Accounts Department

  • Position: Sr. Executive
  • Openings: 1
  • Qualification: M.Com, B.Com
  • Experience: 4–7 years
  • Responsibilities: Handle accounts, taxation, vendor reconciliation, compliance reporting, and financial planning.

3. Production Department

  • Position: Officer
  • Openings: 2
  • Qualification: MSc, B Pharm
  • Experience: 1–3 years
  • Responsibilities: Supervise production operations, ensure adherence to GMP, maintain quality records.
  • Position: Compression Operator
  • Openings: 6
  • Qualification: ITI
  • Experience: 0–5 years
  • Responsibilities: Operate tablet compression machines, monitor process parameters, ensure compliance with SOPs.
  • Position: Granulation Operator
  • Openings: 2
  • Qualification: ITI
  • Experience: 0–5 years
  • Responsibilities: Operate granulation equipment, maintain logs, support process optimization.
  • Position: Strip Operator
  • Openings: 1
  • Qualification: ITI
  • Experience: 0–5 years
  • Responsibilities: Operate strip packing machines, check packaging quality.
  • Position: Coating Operator
  • Openings: 1
  • Qualification: ITI
  • Experience: 0–5 years
  • Responsibilities: Operate coating equipment, monitor coating uniformity, adhere to GMP.
  • Position: Blister Operator
  • Openings: 1
  • Qualification: ITI
  • Experience: 0–5 years
  • Responsibilities: Operate blister packaging machines, maintain records, ensure packaging quality.
  • Position: Capsule Operator
  • Openings: 1
  • Qualification: ITI
  • Experience: 0–5 years
  • Responsibilities: Operate capsule filling machines, monitor yield, troubleshoot minor issues.

Eligibility / Qualifications

  • HR: MBA, BBA, M.Com, B.Com
  • Accounts: M.Com, B.Com
  • Production: MSc, B Pharm, ITI
  • Experience Range: Freshers to 7 years (role-specific)

Location & Salary

  • Walk-in Venue: Sur. 135p, Bavla-Sanand road, Ta-Sanand, Ahmedabad – 382220
  • Date & Time: 5th October 2025 | 9:00 AM to 4:00 PM
  • Salary: Competitive and as per industry standards.

Application Process

Interested candidates are requested to attend the walk-in interview with their updated resume, educational certificates, ID proof, and experience documents.

FAQs

Q1: Who can apply for HR Trainee Officer at Strava Healthcare?
Freshers with MBA, BBA, M.Com, or B.Com qualifications can apply.

Q2: What is the experience requirement for Accounts Sr. Executive role?
Applicants must have 4–7 years of relevant experience in accounts and finance.

Q3: Are ITI candidates eligible for production roles?
Yes, ITI candidates with 0–5 years of experience can apply for various operator positions.

Q4: Where is the walk-in drive taking place?
The drive will be conducted at Bavla-Sanand Road, Ahmedabad, Gujarat.

Q5: What documents should candidates bring to the interview?
Updated resume, academic certificates, ID proof (Aadhar/PAN), and experience letters if applicable.

Summary Table

CompanyStrava Healthcare Pvt. Ltd.
VacanciesMultiple (HR, Accounts, Production)
Required EducationMBA, BBA, M.Com, B.Com, MSc, B Pharm, ITI
Experience0–7 Years (role-specific)

CPC Certified Freshers Openings – Gebbs Healthcare, Aurangabad

Apply now for CPC Certified Medical Coding fresher openings at Gebbs Healthcare Solutions, Sambhajinagar (Aurangabad). B Pharm/M.Pharm eligible.

Kickstart your career in medical coding with Gebbs Healthcare Solutions, one of India’s fastest-growing healthcare outsourcing and revenue cycle management companies. We are hiring CPC Certified freshers at our Sambhajinagar (Aurangabad) facility. If you hold a degree in B Pharmacy or M.Pharmacy and have cleared your CPC certification, this is your chance to secure a high-growth career with a leading healthcare BPO organization.

Unlike generic roles, this opening is designed specifically for certified candidates who want to explore global healthcare processes, compliance management, and advanced medical coding systems.

Company Overview

Gebbs Healthcare Solutions is a trusted leader in healthcare outsourcing services, specializing in medical coding, medical billing, accounts receivable management, and revenue cycle optimization. With over two decades of industry expertise, Gebbs partners with leading hospitals, physician groups, and healthcare organizations across the USA.

Why Choose Gebbs?

  • Globally recognized brand in medical coding and billing
  • Structured training and mentoring programs for freshers
  • Opportunities to work with US healthcare clients
  • CPC-focused roles ensuring career advancement in medical coding
  • Strong emphasis on compliance, accuracy, and HIPAA regulations
  • Consistently ranked among India’s top healthcare BPO employers

Joining Gebbs not only ensures job stability but also helps you build expertise in a high-demand career sector.

Job Role & Responsibilities

The CPC Certified Fresher – Medical Coder role is ideal for candidates looking to enter the healthcare RCM (Revenue Cycle Management) industry.

Key Responsibilities:

  • Review and analyze medical records, physician documentation, and healthcare charts
  • Apply ICD-10, CPT, and HCPCS codes based on CPC certification standards
  • Ensure accuracy and compliance with payer-specific guidelines
  • Work with internal QA teams to minimize coding errors and claim rejections
  • Collaborate with senior coders and managers for continuous learning
  • Maintain strict confidentiality and HIPAA compliance in handling patient data

This position offers freshers the chance to build expertise in international healthcare coding and grow into senior medical coding roles.

Eligibility / Qualifications

  • Education:
    • B Pharmacy, M.Pharmacy, or equivalent life sciences degree
    • CPC Certification (mandatory) from AAPC (American Academy of Professional Coders)
  • Experience:
    • Freshers eligible (0 years experience required)
    • Prior exposure to coding tools, internships, or healthcare projects is an added advantage
  • Skillset Required:
    • Strong knowledge of medical terminology, anatomy, physiology, and pharmacology
    • Proficiency in ICD-10 and CPT guidelines
    • Excellent attention to detail and accuracy
    • Good communication skills and ability to work in team-oriented environments

Location & Salary

Location: Sambhajinagar (Aurangabad), Maharashtra

Salary: Competitive package for freshers in the medical coding domain. Compensation will be aligned with industry standards and CPC certification benefits.

Work Type: Full-time, with structured training sessions and mentoring.

Application Process

Unlike typical walk-in interviews, Gebbs Healthcare Solutions follows a structured recruitment process:

  1. Resume Screening: Candidates must first email their CVs for initial shortlisting.
  2. Interview Scheduling: Selected candidates will be contacted by HR for interview slots.
  3. Assessment Round: Evaluation of coding knowledge, CPC fundamentals, and medical terminology.
  4. Final HR Round: Discussion of compensation, joining formalities, and career path.

How to Apply:

  • Send your updated resume to sagar.nikalje@gebbs.com
  • Mention “Application for CPC Certified Fresher – Medical Coding” in the subject line

Apply today to secure your interview slot! Interviews will be scheduled after resume screening.

FAQs

Q1: Who is eligible to apply for this role?

  • B Pharm or M.Pharm graduates who are CPC Certified. Freshers can apply.

Q2: Is CPC certification mandatory?

  • Yes, only CPC-certified candidates will be considered.

Q3: Is this a walk-in interview?

  • No, interviews will only be scheduled after resume screening.

Q4: What is the career growth path at Gebbs?

  • Freshers typically start as Medical Coders and can grow into Senior Coders, Team Leads, Quality Auditors, and Managers within a few years.

Q5: What salary can CPC freshers expect?

  • Compensation will be industry-aligned, with higher earning potential compared to non-certified coders.

Q6: What makes Gebbs different from other healthcare BPOs?

  • Focus on quality training, global clients, compliance, and career growth opportunities.

Vertical Summary Table

CompanyGebbs Healthcare Solutions
VacanciesCPC Certified Fresher – Medical Coder
Required EducationB Pharmacy, M.Pharmacy, CPC Certification
ExperienceFreshers (0 years)

SCL Lifesciences ARD Hiring | B Pharm/MSc/M.Pharm, Derabassi

SCL Lifesciences Limited, Derabassi is hiring ARD professionals with 2–3 yrs experience in Analytical R&D. Apply today via email.

SCL Lifesciences Limited, a leading player in the pharmaceutical and life sciences sector, is seeking experienced professionals for its Analytical Research & Development (ARD) Department at Bhagwanpura, Derabassi. This opening provides an excellent opportunity for candidates already working in ARD to advance their careers in a dynamic and innovation-focused environment.

Company Overview

SCL Lifesciences Limited is a well-established pharmaceutical company committed to excellence in drug development, analytical research, and manufacturing of high-quality medicines. With a strong focus on innovation, regulatory compliance, and scientific integrity, SCL Lifesciences offers a collaborative work culture and opportunities for professional growth. The company’s ARD department plays a critical role in developing analytical methods, ensuring product quality, and supporting formulation and process development.

Job Role & Responsibilities

Analytical Research & Development (ARD) Professional

  • Develop, validate, and optimize analytical methods for drug substances and formulations.
  • Conduct research on chemical, physical, and biological properties of APIs and formulations.
  • Prepare technical reports, analytical data, and documentation for regulatory submissions.
  • Collaborate with production and QA/QC teams to ensure quality standards.
  • Participate in troubleshooting, method transfer, and technology development projects.
  • Maintain compliance with cGMP, ICH guidelines, and internal SOPs.

Eligibility / Qualifications

  • Education:
    • B Pharm, MSc in Chemistry, M.Pharm
  • Experience: 2–3 years working in the Analytical R&D department.
  • Skills Required:
    • Strong analytical, research, and problem-solving skills.
    • Proficiency in analytical instruments like HPLC, UV-Vis, FTIR, etc.
    • Good documentation and report-writing capabilities.
    • Knowledge of regulatory standards and compliance.

Note: Only candidates currently employed in ARD departments will be considered.

Location & Salary

  • Job Location: Bhagwanpura, Derabassi, Punjab.
  • Salary: Competitive, based on experience and qualifications.
  • Work Mode: Full-time, Onsite.

Application Process

Interested candidates are invited to share their updated resume via email:
manik.mehta@scllifesciences.com

Subject Line Suggestion: Name_ARD_Your Current Company

Apply early to enhance your chances of selection at SCL Lifesciences ARD Department!

FAQs

1. Who can apply for the ARD positions at SCL Lifesciences?
Candidates with B Pharm, MSc (Chemistry), or M.Pharm and 2–3 years of experience in an ARD department.

2. Are freshers eligible?
No, only candidates currently working in ARD with relevant experience will be considered.

3. What kind of work will the ARD professional perform?
They will handle analytical method development, research, documentation, and compliance activities.

4. Where is the job location?
Bhagwanpura, Derabassi, Punjab.

5. How should I apply?
Email your resume to manik.mehta@scllifesciences.com with the suggested subject line.

Summary Table

CategoryDetails
CompanySCL Lifesciences Limited
VacanciesAnalytical Research & Development (ARD)
Required EducationB Pharm, MSc in Chemistry, M.Pharm
Experience2–3 years in ARD department

Rusan Pharma Hiring QA, QC & Production Staff | Ankleshwar

Walk-in at Rusan Pharma, Ankleshwar for QA, QC, Production, and Engineering roles. Open to BSc/MSc/Diploma/BE candidates with 2–10 yrs experience.

Rusan Pharma Ltd., a US FDA-approved API manufacturing facility in Ankleshwar, is inviting applications for multiple positions across Quality Assurance, Quality Control, Production, and Engineering departments. This is an excellent opportunity for pharma professionals with hands-on experience in API manufacturing and GMP compliance to join a globally recognized organization.

Company Overview

Rusan Pharma Ltd. is a leading pharmaceutical company with a state-of-the-art US FDA-approved API manufacturing facility located in Ankleshwar, Gujarat. Renowned for its commitment to quality, innovation, and regulatory compliance, Rusan Pharma produces high-grade APIs for global pharmaceutical markets. The company emphasizes a culture of safety, precision, and continuous learning, making it an ideal workplace for pharma professionals aiming for growth in API manufacturing, QA/QC, and engineering roles.

Job Role & Responsibilities

Quality Assurance (Jr. Officer / Officer / Sr. Officer)

  • Ensure compliance with cGMP, FDA, and ICH guidelines.
  • Implement and monitor QA procedures and SOPs.
  • Conduct audits and support regulatory inspections.
  • Manage documentation, deviations, CAPA, and change control processes.

Production (GMP Coordinator)

  • Oversee API manufacturing operations ensuring adherence to production protocols.
  • Monitor process efficiency and ensure timely completion of batches.
  • Collaborate with QA for process validations and deviations.

Engineering (Officer-Instrumentation / Jr. Officer/Officer Mechanical)

  • Maintain and troubleshoot manufacturing and QC instrumentation.
  • Implement preventive maintenance schedules and ensure operational efficiency.
  • Ensure compliance with equipment qualification and calibration requirements.

Quality Control (Officer/Sr. Officer/Executive / Sr. Executive / Assistant Manager)

  • Perform analysis of raw materials, intermediates, and finished APIs.
  • Handle QMS activities and maintain QC documentation.
  • Supervise laboratory operations and ensure adherence to analytical SOPs.

Eligibility / Qualifications

  • Education:
    • BSc, MSc (Pharmacy, Chemistry, Microbiology, Biotechnology)
    • Diploma/BE Instrumentation, Diploma/BE Mechanical for Engineering roles
  • Experience:
    • QA: 2–10 years in Pharma API QA experience
    • Production: 5–7 years in API manufacturing
    • QC: 4–7 years handling QMS/QC department
    • Engineering: 2–5 years in API manufacturing
  • Skills Required:
    • Strong knowledge of GMP, FDA compliance, and regulatory audits.
    • Hands-on experience in API manufacturing, QA/QC processes, and equipment maintenance.
    • Excellent documentation, analytical, and problem-solving skills.

Location & Salary

  • Location: Rusan Pharma Ltd., Plot No-6406, Nr. Hoechst Chowkdi, GIDC, Ankleshwar, Gujarat – 393002
  • Salary: Competitive, based on qualifications and experience.
  • Work Mode: Full-time, Onsite.

Application Process

Interested candidates are encouraged to share their updated resume via email to the HR team:
mitesh.maharaj@rusanpharma.com | monika.prajapati@rusanpharma.com

Include the position in your email subject line for faster processing.

Apply early to secure your spot at this US FDA-approved API manufacturing facility!

FAQs

1. Who can apply for Rusan Pharma vacancies?
Candidates with BSc/MSc in life sciences, Diploma/BE in Engineering with 2–10 years of relevant experience.

2. Are freshers eligible?
No, the positions require prior experience in API manufacturing, QA/QC, or engineering.

3. Which departments are hiring?
Quality Assurance, Production, Quality Control, and Engineering.

4. Where is the facility located?
Ankleshwar, Gujarat, at GIDC Plot No-6406 near Hoechst Chowkdi.

5. How do I apply?
Send your updated resume via email to mitesh.maharaj@rusanpharma.com or monika.prajapati@rusanpharma.com.

Summary Table

CategoryDetails
CompanyRusan Pharma Ltd.
VacanciesQA (Jr. Officer/Officer/Sr. Officer), QC (Officer/Sr. Officer/Executive), Production (GMP Coordinator), Engineering (Officer-Instrumentation, Jr. Officer/Officer Mechanical)
Required EducationBSc/MSc (Pharmacy, Chemistry, Microbiology, Biotechnology), Diploma/BE Instrumentation/Mechanical
Experience2–10 years (depending on department and role)

Clinical Research Project Manager Vacancy | HRAPL Nagpur

HRAPL is hiring Clinical Research Project Managers in Nagpur. Apply with 3–4 years’ experience in life sciences. Full-time onsite role.

HRAPL, a trusted name in clinical research and site management, is inviting applications for the position of Project Manager. This opportunity is ideal for professionals passionate about advancing their careers in the field of clinical research. With a focus on site management excellence and regulatory compliance, HRAPL offers an enriching work environment that fosters professional growth.

Company Overview

HRAPL (Healthcare Research and Project Logistics) is a reputed clinical research organization (CRO) providing specialized services in site management, project coordination, regulatory compliance, and clinical trial monitoring. The company is committed to improving healthcare outcomes by supporting global pharmaceutical and biotechnology companies in conducting ethical, high-quality clinical trials. With a strong presence in India, HRAPL ensures integrity, patient safety, and data accuracy across all projects.

Job Role & Responsibilities

As a Project Manager in Clinical Research, you will play a vital role in ensuring smooth execution of clinical trials. Your responsibilities include:

  • Overseeing clinical trial projects from initiation to close-out.
  • Coordinating with site teams, investigators, and sponsors.
  • Ensuring compliance with ICH-GCP guidelines, regulatory frameworks, and SOPs.
  • Monitoring project timelines, deliverables, and budget utilization.
  • Leading and mentoring project coordinators and site staff.
  • Managing risk, quality issues, and operational challenges during clinical trials.
  • Reporting project progress and preparing regulatory documentation.

Eligibility / Qualifications

  • Education: Bachelor’s or Master’s degree in Life Sciences, Medical Sciences, Pharmacy, Biotechnology, Clinical Research, or related fields.
  • Experience: Minimum 3–4 years as a Project Manager or Project Coordinator in clinical research.
  • Key Skills:
    • Strong organizational and leadership capabilities.
    • Excellent communication and interpersonal skills.
    • Proficiency in project management tools and clinical trial documentation.
    • Ability to manage cross-functional teams and ensure quality outcomes.

Location & Salary

  • Job Location: Nagpur (Full-time, Onsite).
  • Salary: Competitive, based on experience and qualifications.

Application Process

Interested candidates may share their updated resume via email:
contact@hrapl.in

Subject Line Format: Name_PM/PC_Your Location

For more information, visit: www.hrapl.in

Apply early to secure your chance to work with a leading CRO in India!

FAQs

1. Who can apply for the Project Manager role at HRAPL?
Candidates with a Bachelor’s/Master’s in Life Sciences, Pharmacy, Biotechnology, or Clinical Research and 3–4 years of relevant experience.

2. Is this role open to freshers?
No, only candidates with prior experience in clinical research project management or coordination can apply.

3. What skills are required for this role?
Strong leadership, communication, organizational skills, and knowledge of GCP guidelines are essential.

4. Where is this role based?
Nagpur, Maharashtra (Full-time, Onsite).

5. How should I apply?
Send your resume to contact@hrapl.in with the subject line Name_PM/PC_Your Location.

Summary Table

CategoryDetails
CompanyHRAPL (Healthcare Research and Project Logistics)
VacanciesProject Manager (Clinical Research)
Required EducationBachelor’s/Master’s in Life Sciences, Pharmacy, Biotechnology, Clinical Research
ExperienceMinimum 3–4 years as Project Manager/Coordinator in Clinical Research

B Pharm/MSc Quality Control & Assurance Vacancies at CORONA Remedies, Ahmedabad

Walk-in interview at CORONA Remedies Ltd, Ahmedabad for B Pharm/MSc candidates with 4–8 years’ experience in Quality Control & Quality Assurance. Apply now!

CORONA Remedies Limited, one of India’s fastest-growing pharmaceutical companies, is conducting a walk-in interview for experienced professionals in Quality Control (QC) and Quality Assurance (QA) departments. This is an excellent opportunity for B Pharm and MSc graduates with 4–8 years of experience in the pharma industry to advance their careers with a trusted name in healthcare.

Company Overview

CORONA Remedies Limited is a well-established pharmaceutical company headquartered in Ahmedabad, Gujarat. With a strong presence across therapeutic segments, CORONA is known for its commitment to innovation, quality, and affordability. The company’s state-of-the-art manufacturing facilities comply with global standards, ensuring the highest level of quality in every product. CORONA Remedies continues to contribute to healthcare advancement with its diverse portfolio of formulations.

Job Role & Responsibilities

Quality Control (QC)

  • Operate and manage laboratory instruments including HPLC, Dissolution Apparatus, DT Apparatus, Analytical Balance, Friability & Hardness Testers, FTIR, and UV-Spectrophotometer.
  • Conduct analysis of raw materials, in-process samples, finished products, and stability testing.
  • Perform process validation and participate in lab incidents, OOS (Out of Specification), OOT (Out of Trend), and analytical deviation investigations.

Quality Assurance (QA)

  • Review specifications, methods of analysis, and analytical protocols.
  • Handle OOS/OOT investigations and laboratory events.
  • Review and approve Quality Control documentation.
  • Demonstrate knowledge of qualification and validation activities.
  • Oversee IPQA (In-Process Quality Assurance) activities in OSD (Oral Solid Dosage) plants.

Eligibility / Qualifications

  • Education: B Pharm, MSc (Pharmaceutical Chemistry, Quality Assurance, Industrial Pharmacy, or related disciplines).
  • Experience: 4–8 years in pharmaceutical Quality Control or Quality Assurance.
  • Skills Required:
    • Strong knowledge of analytical techniques and regulatory requirements.
    • Familiarity with GMP guidelines and pharma documentation.
    • Ability to handle deviations and investigations effectively.

Location & Salary

  • Job Location: CORONA Remedies Limited, Plot No. 503, Village Bhayla, Near Super Gas, Bavla-Bagodara Highway, Ahmedabad.
  • Interview Venue: CORONA Remedies Limited, Block “S”, Mondeal Business Park, Near Gurudwara, S.G Highway, Ahmedabad.
  • Interview Date & Time: 05th October 2025 | 10:00 AM – 03:00 PM.
  • Salary: Competitive, based on qualifications and experience.

Application Process

Candidates interested in advancing their careers with CORONA Remedies can attend the walk-in interview on the specified date and venue.

If unable to attend in person, applicants may send their updated resumes to: hr.bhayla@coronaremedies.com.

Apply before 5th October 2025 to secure your spot!

FAQs

1. Who can apply for these positions?
B Pharm and MSc graduates with 4–8 years of experience in pharmaceutical Quality Control or Quality Assurance.

2. What is the mode of selection?
Walk-in interview at the Ahmedabad office on 05th October 2025.

3. Can I apply if I cannot attend the walk-in?
Yes, you can send your updated CV to hr.bhayla@coronaremedies.com.

4. What skills are preferred for this role?
Hands-on experience with analytical instruments, strong documentation knowledge, and expertise in OOS/OOT handling and GMP compliance.

5. Is this role suitable for freshers?
No, only candidates with 4–8 years of relevant experience will be considered.

Summary Table

CategoryDetails
CompanyCORONA Remedies Limited
VacanciesQuality Control & Quality Assurance (Multiple positions)
Required EducationB Pharm, MSc (Pharmaceutical Chemistry, Industrial Pharmacy, QA, etc.)
Experience4–8 years in QC/QA roles

Formulation Development R&D – 2-6 Yrs – Bangalore

Arcolab hiring Formulation Development professionals – 2-6 yrs experience – R&D, Bangalore. Apply now to join innovative pharma research.

Advance your career in pharmaceutical R&D with Arcolab, a leading innovator in formulation development. We are seeking experienced professionals to join our Bangalore R&D team, contributing to product optimization, transfer projects, and regulatory documentation. This is an excellent opportunity for candidates passionate about pharmaceutical research, product development, and quality-driven operations.

Company Overview

Arcolab Pvt. Ltd., based in Bangalore, is a recognized pharmaceutical organization focused on innovative drug development, formulation optimization, and regulatory-compliant manufacturing. With a strong emphasis on research and development, Arcolab provides professionals the opportunity to work on cutting-edge projects in collaboration with global CMOs and regulatory bodies. Employees benefit from a collaborative environment, exposure to advanced formulation technologies, and a clear path for career growth in pharma R&D.

Job Role & Responsibilities

Position: Formulation Development – R&D
Experience: 2-6 Years
Location: Bangalore

As a Formulation Development professional, your role will involve:

  • Reviewing and understanding product technicalities from internal sites to ensure smooth transfer to external CMOs.
  • Handling investigations related to OOS (Out of Specification), OOT (Out of Trend), and deviations reported during new product development or site transfer projects.
  • Conducting feasibility trials and scale-up trials for new and existing formulations.
  • Managing product robustness projects, including execution and monitoring of optimization batches and registration/commercial batches for PR projects.
  • Reviewing APQR (Annual Product Quality Review), RCI (Root Cause Investigation), CAPA (Corrective and Preventive Actions), PDR (Product Development Report), and other related documents.
  • Preparing and reviewing essential documentation such as MFRs (Master Formula Records), BMRs (Batch Manufacturing Records), BPRs (Batch Packaging Records), protocols, and reports for trials, feasibility studies, purchase orders, and new product batches.
  • Reviewing and approving PVP (Product Validation Protocol) and PVR (Product Validation Report) to ensure regulatory compliance and quality standards.

Key Skills & Expertise:

  • Strong knowledge of pharmaceutical formulation development, scale-up, and transfer projects.
  • Hands-on experience in preparing and reviewing regulatory and quality documentation.
  • Ability to conduct feasibility and robustness trials for various batch sizes.
  • Familiarity with CAPA, RCI, and APQR processes.
  • Excellent analytical, documentation, and problem-solving skills.

Eligibility / Qualifications

  • Education: B Pharm, M.Pharm, or related life sciences background.
  • Experience: 2-6 years in pharmaceutical R&D, formulation development, and product transfer projects.
  • Preferred: Candidates with experience in handling OOS/OOT investigations, CAPA, and regulatory documentation.

Relevant courses and areas of expertise: Pharmaceutical Formulation, Drug Development, Regulatory Compliance, Quality Assurance, Product Development, APQR, CAPA, Feasibility & Scale-up Trials.

Location & Salary

  • Job Location: Bangalore, India
  • Salary: Competitive and based on experience
  • Joining: Immediate or as per mutual agreement

Application Process

Candidates who meet the qualifications and are passionate about formulation development are encouraged to apply immediately:

  • Email your profile: Navya@arcolab.com
  • CTA: Apply now to join an innovative pharmaceutical R&D team and contribute to cutting-edge formulation projects!

FAQs

Q1: What is the required educational qualification?
A: B Pharm, M.Pharm, or related life sciences degree.

Q2: What is the experience range for this position?
A: 2-6 years in formulation development and R&D.

Q3: What kind of projects will the candidate handle?
A: Product transfer to CMOs, feasibility trials, robustness studies, optimization batches, and regulatory documentation.

Q4: Where is the job located?
A: Bangalore, India.

Q5: How do I apply?
A: Send your CV to Navya@arcolab.com.

Summary Table

CategoryDetails
CompanyArcolab Pvt. Ltd.
VacanciesMultiple – Formulation Development
Required EducationB Pharm, M.Pharm, or related
Experience2-6 years

MSc, B Pharm, Diploma Vacancies at Felix Generics – Walk-in Baddi 2025
Attend walk-in interview at Felix Generics for multiple vacancies (MSc, B Pharm, Diploma) on 5th October 2025 in Baddi for Pithampur plant roles.

Felix Generics Pvt. Ltd., a trusted name in pharmaceutical manufacturing, is conducting a Walk-In Interview in Baddi on 5th October 2025 (Sunday) for various positions at their USFDA-approved Pithampur Plant (SEZ, Phase II, District Dhar, Madhya Pradesh). This is a golden opportunity for pharma professionals with expertise in Injectables, OSD, Quality Control, Engineering, and Technology Transfer to advance their careers with a leading global generics company.

Company Overview

Felix Generics Pvt. Ltd. is part of a reputed pharmaceutical group with global recognition in formulations, injectables, and technology-driven healthcare solutions. With a strong focus on compliance, innovation, and regulatory approvals such as USFDA and EUGMP, Felix Generics continues to strengthen its position in the international generics market. The company offers robust career growth, exposure to international quality standards, and an opportunity to contribute to global healthcare.

Job Role & Responsibilities

Felix Generics is hiring for multiple departments and designations. Candidates with relevant educational qualifications and experience in USFDA/EUGMP-approved units will be prioritized.

1. Production (Injectables)

  • Designation: Officer to Executive
  • Experience: 4–6 years
  • Qualification: MSc (Pharma/Science)
  • Responsibilities:
    • Supervision of aseptic process activities.
    • Troubleshooting in aseptic operations (NVPC failure, power failure, remediation action plans).
    • SOP preparation.
    • Experience in aseptic filling operations in sterile facilities.

2. Production Technicians (Injectables)

  • Designation: Technician
  • Experience: 4–6 years
  • Qualification: Diploma (Pharma/Science)
  • Responsibilities:
    • Dispensing & compounding process.
    • Visual inspection & packing line operations.
    • Preference: Microsphere Dry Powder Injectable exposure.

3. Quality Control (Injectables)

  • Designation: Officer to Sr. Executive
  • Experience: 2–8 years
  • Qualification: MSc
  • Responsibilities:
    • Handling HPLC, GC, FTIR, UV.
    • RM, water, PP stability testing.
    • Calibration and analysis of samples.

4. Engineering (OSD/Injectables)

  • Designation: Officer/Sr. Officer (Plant Maintenance)
  • Experience: 4–8 years
  • Qualification: BE (Electrical/Mechanical)
  • Responsibilities:
    • Preventive & breakdown maintenance of process equipment.
    • Documentation, protocols, and quality records.
  • Designation: Technician/Sr. Technician (Plant Maintenance)
  • Experience: 6–8 years
  • Qualification: Diploma (Electrical/Mechanical)
  • Responsibilities:
    • Equipment maintenance for OSD/Injectable plants.
  • Designation: Technician/Sr. Technician (Water System/HVAC)
  • Experience: 4–8 years
  • Qualification: Diploma (Mechanical/Electrical)
  • Responsibilities:
    • Operation & maintenance of HVAC/water systems.

5. Technology Transfer (Injectables)

  • Designation: Sr. Officer to Sr. Executive
  • Experience: 5–8 years
  • Qualification: B Pharm/M.Pharm
  • Responsibilities:
    • Execution of validation batches.
    • Preparation & review of SOPs.

6. Quality Control (QC Validation & Analytical)

  • QC Validation Analyst (Br. Officer to Sr. Executive)
    • Experience: 3–8 years
    • Qualification: MSc/M.Pharm
    • Responsibilities: Method validation, transfer, cleaning validation, report review.
  • QC Sr. Officer to Executive
    • Experience: 4–7 years
    • Expertise: HPLC, GC, FTIR analysis.

7. IPQA

  • Designation: Officer to Executive
  • Experience: 2–8 years
  • Qualification: B Pharm/M.Pharm
  • Responsibilities:
    • In-process checks, batch record review, FG sample inspection.

8. Analytical QA

  • Designation: Executive to Sr. Executive
  • Experience: 1–10 years
  • Qualification: B Pharm/M.Pharm/BSc
  • Responsibilities:
    • Review of analytical data, deviation handling, instrument qualification.

9. Production (OSD – Granulation, Compression, Packing)

  • Designation: Officer to Executive
  • Experience: 2–5 years
  • Qualification: M.Pharm/B Pharm
  • Responsibilities:
    • Granulation, compression, liquid filling, primary bottle packing.
    • SAP system handling, deviation/change control.

10. Technician – OSD Production

  • Designation: Technician
  • Experience: 2–6 years
  • Qualification: Diploma/D.Pharm
  • Responsibilities:
    • Granulation & compaction.
    • Liquid manufacturing & filling.
    • Primary bottle packing (CVC Line).

Eligibility / Qualifications

  • B Pharm, M.Pharm, MSc, BSc, Diploma, BE (Electrical/Mechanical).
  • Experience: 0–10 years (depending on role).
  • Mandatory: Candidates with experience in USFDA/EUGMP-approved facilities will be given preference.
  • Good communication and documentation skills required.

Location & Salary

  • Plant Location: Pithampur, SEZ, Madhya Pradesh.
  • Walk-In Venue: MG Regency Hotel, National Highway 21A, Kalka-Baddi Road, Baddi, Himachal Pradesh – 173205.
  • Date & Time: 5th October 2025 (Sunday), 09:30 AM – 03:30 PM.
  • Salary: As per industry standards; competitive package based on experience.

Application Process

Interested candidates should attend the walk-in interview in person with updated CV, educational certificates, experience documents, and ID proof.

For queries, contact:

Apply early to secure your spot in the selection process!

FAQs

Q1: Who can attend the Felix Generics walk-in interview?
Candidates with B Pharm, M.Pharm, MSc, Diploma, or BE qualifications and relevant pharma experience can attend.

Q2: Is prior USFDA-approved plant experience mandatory?
It is highly preferred, especially for production and QC roles.

Q3: Where is the walk-in venue located?
MG Regency Hotel, National Highway 21A, Kalka-Baddi Road, Baddi, Himachal Pradesh – 173205.

Q4: What documents should I carry for the interview?
Updated CV, educational certificates, experience documents, ID proof, and recent photographs.

Q5: How can I apply if I cannot attend in person?
You can share your profile via email at jobs@felixvet.com.

Summary Table

CompanyFelix Generics Pvt. Ltd.
VacanciesMultiple (Production, QC, QA, Engineering, IPQA, Technology Transfer)
Required EducationB Pharm, M.Pharm, MSc, BSc, Diploma, BE (Electrical/Mechanical)
Experience0–10 years (depending on role)

Jr. Officer Purchase Vacancy for Science Graduates | Zytex Biotechnology Baroda

Apply for Jr. Officer Purchase at Zytex Biotechnology in Baroda. Open for Science graduates with 0–2 years’ experience. Salary up to 3 LPA.

Zytex Biotechnology Pvt. Ltd., a reputed name in biotechnology and life sciences, is inviting applications for the position of Jr. Officer – Purchase at its Baroda unit. This is an excellent opportunity for science graduates looking to build their career in procurement and supply chain management within the biotech sector. With a competitive salary package and growth prospects, this role offers a strong career foundation for freshers and young professionals.

Company Overview

Zytex Biotechnology Pvt. Ltd. is a leading biotech company with a strong presence in enzymes, probiotics, and life sciences innovations. Over the years, Zytex has established itself as a trusted name in biotechnology solutions, supporting pharmaceutical, food, and healthcare industries. With a focus on research, innovation, and customer satisfaction, Zytex offers employees a dynamic and growth-oriented work environment.

Job Role & Responsibilities

As a Jr. Officer – Purchase, you will play an essential role in the company’s procurement and supply chain operations. Key responsibilities include:

  • Assisting in vendor selection, negotiations, and purchase order processing
  • Coordinating with suppliers for timely delivery of raw materials and goods
  • Ensuring compliance with procurement policies and documentation standards
  • Maintaining purchase records, invoices, and supporting documents
  • Supporting senior purchase officers in daily operations and audits
  • Building vendor relationships to ensure cost-effective and quality sourcing

This role is ideal for candidates eager to develop expertise in procurement within the biotech and pharmaceutical domain.

Eligibility / Qualifications

  • Education: Graduate degree (Science background preferred) – BSc. in Biotechnology, Microbiology, Biochemistry, Life Sciences, or related fields
  • Experience: 0–2 years (Freshers with strong academic background can apply)
  • Preferred Skills:
    • Basic knowledge of supply chain and procurement
    • Good communication and negotiation skills
    • Proficiency in MS Office tools
    • Strong organizational and analytical abilities

Location & Salary

  • Location: Baroda, Gujarat (local candidates preferred)
  • Salary: Up to INR 3 LPA (based on qualifications and experience)

Application Process

Interested candidates can apply by sharing their updated profile via email at hr2.baroda@zytex.com.

Apply early to secure your spot, as this opportunity may close soon!

FAQs

1. Who can apply for this role?
Science graduates with 0–2 years’ experience, preferably from Baroda or nearby regions.

2. Is prior procurement experience mandatory?
No, freshers are also encouraged to apply.

3. What is the expected salary range?
The salary offered is up to INR 3 LPA, depending on experience and qualifications.

4. Are local candidates preferred?
Yes, Zytex has mentioned that local candidates will be given priority.

5. What is the career growth in this role?
Jr. Officers can progress to Officer/Sr. Officer roles in procurement, supply chain, or operations based on performance.

Summary Table

CompanyZytex Biotechnology Pvt. Ltd.
VacanciesJr. Officer – Purchase
Required EducationGraduate (Science background preferred – BSc. Biotechnology, Microbiology, Biochemistry, Life Sciences)
Experience0–2 years (Freshers eligible)

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