Quality Control Officer - Microbiology | Lupin Pharmaceuticals | Pune, MH, India
Job Summary
Join Lupin Pharmaceuticals in Pune as a Quality Control Officer specializing in Microbiology. This role is crucial for ensuring cGMP compliance within our state-of-the-art biotech facility. The ideal candidate will have hands-on experience in environmental monitoring, water testing (Bioburden, BET, Sterility), and validation activities. We are seeking a motivated Post Graduate in Microbiology or Biotechnology looking to advance their career in a dynamic pharmaceutical environment.
Available Position Description:
Designation: Quality Control Officer
Location: Pune, Maharashtra, India
Employment Type: Full-Time (Experienced Professional)
Education: Post Graduation (M.Sc./M.Tech) in Microbiology or Biotechnology.
Work Experience: 1 to 5 years of relevant quality control experience within the Pharmaceutical or Biotechnology industry.
Key Responsibilities
As a QC Officer focusing on microbiological activities, your responsibilities will include:
- Environmental Monitoring: Performing routine environmental monitoring (EM) of all classified areas within the Drug Product (DP) manufacturing facility.
- Media Management: Preparation of media required for utility monitoring and area monitoring, ensuring compliance with protocols.
Lab Operations & Testing:
- Conducting routine sampling and testing of water samples and compressed air.
- Performing Bioburden, Bacterial Endotoxin Test (BET), and Sterility testing.
- Operating and calibrating daily lab equipment, including pH meters, balances, autoclaves, DHS units, incubators, air samplers, and particle counters.
- Culture Management: Executing sub culturing, serial dilution of standard cultures, Growth Promotion Tests (GPT), and identification of isolates.
- Validation & Documentation: Executing validation, qualification, and re-qualification activities strictly as per approved protocols.
Essential Skills & Knowledge
Strong theoretical and practical knowledge of all microbiological related activities in a QC setting.
Familiarity with regulatory documentation and quality management systems: cGMP, Change Control, Deviations, OOS investigations, Sample Management, Stability Management, and standard investigation tools (e.g., root cause analysis).
How To Apply:
2.Register using your email ID and create a login.
3.Fill in your personal and educational details accurately.
4.Upload your updated resume in PDF format.
5. Submit it.
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