Lupin Limited, one of India’s leading pharmaceutical companies with a strong global presence, has announced current vacancies at its Mandideep (Bhopal) manufacturing facility. The organization is inviting applications from qualified and experienced professionals across Quality Control, Microbiology, Production, Analytical QA, Warehouse, Engineering Store, and Utility departments.

Candidates with exposure to USFDA, MHRA, and other international regulatory environments will have an added advantage. This recruitment drive offers excellent opportunities for freshers as well as experienced professionals looking to build a career in a regulated pharmaceutical manufacturing environment.

Available Departments and Positions

1. Quality Control (API)

Designation: Associate / Officer / Executive

Qualification: B.Pharm, B.Sc, M.Sc

Experience: 2–12 Years

Key responsibilities include:

HPLC, GC, LCMS operation and analysis

Raw material, intermediate, and API testing

Method validation and method transfer

OOS, OOT investigations

Instrument qualification and calibration

Pharmacopoeial compliance activities

2. Quality Control (Microbiology – API)

Designation: Officer

Qualification: M.Sc Microbiology

Experience: 2–6 Years

Key responsibilities include:

Media preparation and sterilization

Water sample analysis

Environmental monitoring

Microbiological testing

Stability and validation sample testing

Data integrity and cGMP compliance

3. Production (API)

Designation: Associate / Jr. Officer / Officer

Qualification: Diploma Chemical, B.Sc, M.Sc Chemistry

Experience: Freshers to 12 Years

Responsibilities include:

Batch processing operations

Shop-floor manufacturing activities

Equipment operation and monitoring

Online documentation and BPR filing

SAP-related activities

GMP compliance in production areas

4. Analytical QA (FML)

Designation: Officer

Qualification: B.Pharm

Experience: 2–6 Years

Responsibilities include:

Analytical data review

Laboratory investigations

Change control management

Audit trail review

Method validation review

GLP and GMP compliance monitoring

5. Warehouse (API)

Designation: Executive

Qualification: B.Com, M.Com, B.Sc, M.Sc

Experience: 7–12 Years

Responsibilities include:

Material receipt and dispatch

Inventory management

Warehouse compliance activities

Documentation control

GMP and GDP adherence

Coordination with cross-functional teams

6. Engineering Store

Designation: Trainee Associate / Trainee Officer

Qualification: B.Com, M.Com, B.Sc, M.Sc

Experience: Freshers & Experienced

Responsibilities include:

Engineering store operations

SAP GRN processing

Material receipt and issue

Inventory control

Vendor coordination

Engineering documentation management

7. Utility (API)

Designation: Executive

Qualification: B.E. Mechanical

Experience: 7–12 Years

Responsibilities include:

Utility system maintenance

HVAC and compressed air systems

Chilled water and cooling systems

Preventive and breakdown maintenance

Regulatory compliance

Equipment qualification activities

Important Eligibility Criteria

Candidates with USFDA and MHRA regulatory exposure will be preferred.

Applicants having less than five years of experience must possess a minimum of 60% academic marks.

Candidates should not have attended a Lupin interview during the last six months.

Why Join Lupin?

Lupin is recognized globally for its commitment to quality, innovation, and regulatory excellence. Employees gain exposure to advanced pharmaceutical technologies, international regulatory standards, and structured career development programs. Working at the Mandideep facility provides valuable experience in API manufacturing and quality systems aligned with global compliance requirements.

Application Process

Interested candidates can share their updated profiles to:

parichaymdp@lupin.com

Chetanchouhan@lupin.com

Candidates should mention the department and position applied for in the email subject line for faster processing.

Technical FAQs

1. What analytical instruments are commonly used in API Quality Control laboratories?

API QC laboratories routinely use HPLC, GC, LC-MS/MS, UV-Visible Spectrophotometers, Dissolution Testers, FTIR, and Karl Fischer titrators for testing raw materials, intermediates, and finished APIs.

2. What is the difference between OOS and OOT results?

OOS (Out of Specification) occurs when test results fall outside predefined acceptance criteria, while OOT (Out of Trend) refers to unexpected variations from historical data trends despite being within specifications.

3. Why is method validation important in pharmaceutical analysis?

Method validation ensures that an analytical method consistently produces accurate, precise, specific, robust, and reliable results as required by ICH and regulatory guidelines.

4. What is Environmental Monitoring in a microbiology laboratory?

Environmental Monitoring (EM) is the systematic assessment of air, surfaces, personnel, and water systems to ensure controlled manufacturing environments meet microbiological quality requirements.

5. What is the role of HVAC systems in pharmaceutical manufacturing?

HVAC systems maintain temperature, humidity, pressure differentials, and air cleanliness levels, helping prevent contamination and ensuring compliance with GMP requirements for product quality and patient safety.