Lupin Pharmaceuticals Hiring For Quality Control Officer - Pune Maharashtra

Quality Control Officer - Microbiology | Lupin Pharmaceuticals | Pune, MH, India

Lupin Pharmaceuticals Hiring For Quality Control Officer - Pune Maharashtra
Lupin Pharmaceuticals Hiring For Quality Control Officer - Pune Maharashtra


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: 

1.Click here For 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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