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, BSc. or MSc. 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
- BSc. / MSc. 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
