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Sun Pharma QC Analyst Job For MSc Biotech, Microbiology, Apply Online
Title: Officer – Microbiology
Date: Mar 10, 2025
Location: Dewas SGO – Plant
Company: Sun Pharmaceutical Industries Ltd
Job Description
Position: QC Analyst
Department: Quality Control
Designation: Officer / Sr. Officer
Education Qualification: M.Sc. in Biotechnology, Chemistry, or Microbiology
Total Years of Experience: 2 – 4 Years
Job Role: QC Analyst
Responsibilities:
- Ensure compliance with cGMP and safety standards in the Quality Control Lab.
- Prepare and use microbiological media and reagents, ensuring the availability of prepared/qualified media for routine lab usage.
- Conduct calibration of laboratory equipment/instruments.
- Maintain laboratory equipment, inventory, and supplies.
- Ensure the integrity, accuracy, and adequacy of the analysis performed.
- Maintain document issuance, retrieval, and arrangement with complete traceability.
- Ensure compliance with cGMP and safety standards in Central Quality Control, Stability, Microbiology Lab, and Packaging Lab.
- Execute and facilitate daily GLP and instrumentation activities in Central Quality Control, Stability, Microbiology Lab, and Packaging Lab.
- Responsible for calibration (In-House and External) of analytical instruments in Central Quality Control, Stability, Microbiology Lab, and Packaging Material Lab.
- Manage reference standards, primary standards, lab chemicals, and lab stationery, along with associated activities.
- Ensure the timely preparation and standardization of lab reagents and volumetric solutions in Central Quality Control, Stability, Microbiology Lab, and Packaging Material Lab.
- Maintain the availability of lab chemicals, lab stationery, and other lab-related items in Central Quality Control, Stability, Microbiology Lab, and Packaging Lab.
- Prepare and review schedules/planners for In-House Calibration, External Calibration, PPV-PTS, and PPV-SPR.
- Prepare and maintain Calibration Standards/Primary Standards as required.
- Ensure timely completion of periodic calibration of laboratory instruments and associated activities.
- Coordinate with stakeholders and vendors for timely completion of GLP and instrumentation-related activities.
- Document analytical data and calculate results.
- Ensure the accuracy of documents and maintain neat, concise, and organized analytical/activity data.
- Perform additional activities as required.
- Ensure compliance with cGMP requirements and laboratory procedures.
- Coordinate with external vendors for calibration/preventive maintenance activities when required.
- Ensure cGMP and GDP compliance during routine work.
- Maintain integrity, accuracy, and adequacy in all performed activities.
- Be accountable for all activities related to instruments, GLP, qualification, and documentation.
- Ensure contamination control is implemented and followed at the site per Contamination Control Strategy (CCS) and respective procedures.
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