Malladi walk-in Production, QA, QC
- Company Overview
- Job Role & Responsibilities
- Production – API Manufacturing
- Quality Assurance (QA)
- Quality Control (QC)
- Engineering Services (Electrical & Mechanical)
- Eligibility / Qualifications
- Required Educational Background
- Experience Requirements
- Required Skills
- Location & Salary
- Job Location
- Salary
- Walk-In Interview Details
- Documents to Carry
- Application Process
- Why Build a Career in API Pharmaceutical Manufacturing
- Frequently Asked Questions (FAQs)
- Who can attend the Malladi Drugs walk-in interview?
- Are freshers eligible for the production department?
- What departments are hiring in this recruitment drive?
- Where will the selected candidates work?
- How can candidates apply if they cannot attend the walk-in interview?
- Job Summary
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:
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 |

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