Lupin Walk-in Interview for Quality Control, Quality Assurance, and Manufacturing

Lupin, a globally renowned pharmaceutical company, invites experienced professionals to a walk-in interview for multiple openings in Quality Control (QC), Quality Assurance (QA), and Manufacturing (Biosimilars) at its state-of-the-art facility in Ghotawade, Pune. This is your chance to become part of one of the fastest-growing pharma companies, contributing to cutting-edge biosimilar development and high-quality drug manufacturing.

If you have 2 to 10 years of relevant experience and hold qualifications such as B.Pharm, M.Pharm, B.Tech, B.Sc. or M.Sc. in Microbiology, Biotechnology, or Chemistry, we welcome you to join this recruitment drive and take the next step in your professional journey.

Walk-in Interview Details

Date: Sunday, June 1, 2025

Time: 08:30 AM – 06:00 PM (Registration closes at 12:00 PM sharp)

Venue: Hotel Pride, 5, University Road, Narveer Tanaji Wadi, Shivajinagar, Pune, Maharashtra 411005

Job Location: Lupin Biotech Campus, Ghotawade, Pune

Open Positions & Department-wise Details

1. Quality Assurance (QA)

Join Lupin’s QA team and ensure compliance across biopharmaceutical operations.

Key Responsibilities:

• In-process quality assurance (IPQA)
• Review of BMR, BPR, and other GMP documentation
• Execution and monitoring of Quality Management Systems (QMS)
• Handling of deviation, CAPA, and change controls
• Ensuring regulatory compliance and audit preparedness

Required Skills:

Strong command over GMP guidelines

Experience in QA-QMS, document control, and regulatory readiness

2. Quality Control (QC)

Be a part of Lupin’s robust QC function focused on analytical excellence.

Key Responsibilities:

• Analytical testing using HPLC, Electrophoresis, and other sophisticated tools
• Experience in Microbiology and Stability Studies
• Sampling, testing, and documentation in accordance with cGMP norms
• Data analysis and report generation for product batches

Required Skills:

Proficiency in instrument handling, data integrity, and analytical reporting

Familiarity with Pharmacopoeial standards

3. Biosimilars Manufacturing – Upstream & Downstream

Work at the forefront of biotechnology and large-scale biologics production.

Key Responsibilities – Upstream:

• Handling single-use and stainless-steel bioreactors
• Media preparation, inoculum development, and fermentation

Key Responsibilities – Downstream:

• Operation of chromatography systems for protein purification
• Buffer preparation and column packing/unpacking

Required Skills:

Hands-on experience with bio-process equipment

Knowledge of cGMP practices in biologics production

🎓 Eligibility Criteria

Qualification Specialization

• B.Pharm / M.Pharm Pharmacy
• B.Tech / M.Tech Biotechnology / Bioprocess
• B.Sc. / M.Sc. Microbiology / Biotechnology / Chemistry

Experience: Minimum 2 years, maximum 10 years in a relevant domain

Industry Preference: Prior experience in biopharma, sterile, or biosimilar operations is highly desirable

Contact & Additional Info

If you are unable to attend the walk-in, you may share your CV at:

📧 careers.biotech@lupin.com