Lupin Pharmaceuticals Hiring For Quality Control Officer - Pune Maharashtra

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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