Officer - Microbiology

**Title**:Officer - Microbiology**:

- Date: Mar 10, 2025
- Location: Dewas SGO - Plant
- Company: Sun Pharmaceutical Industries Ltd

**Position**:QC Analyst

**Department**:Quality Control

**Designation**:Officer / Sr. Officer

**Education Qualification**:M.Sc. in Biotechnology or Chemistry or Microbiology

**Total Years of Experience**:2 - 4 Years

**Job Role**:QC Analyst

**Responsibilities**:

- Ensure compliance to cGMP and safety standards in the Quality Control Lab.
- Preparations & usage of microbiological media and Reagents etc. and ensure always availability of prepared/qualified media for routine usage in Lab.
- Conduct Calibration of laboratory equipment/instruments.
- Maintain laboratory equipment, inventory and supplies.
- Ensure integrity, accuracy and adequacy of the analysis performed.
- Maintain documents issuance, retrieval and arrangement with complete traceability. Ensure compliance to cGMP and safety standards in Central Quality Control, Stability, Microbiology Lab. and Packaging Lab.
- To ensure, execute and facilitate daily GLP and Instrumentation activities pertaining to Central Quality Control, Stability, Microbiology Lab. and Packaging Lab.
- Responsible for calibration (In-House and External Calibration) of Analytical instrument in Central Quality Control, Stability, Micro. Lab. and Packaging Material Lab.
- Management of reference standard, primary standard, lab chemicals, lab stationary etc. and its associated activities.
- To ensure timely preparation and standardization of lab reagents and volumetric Solutions in Central Quality Control, Stability, Microbiology Lab. and Packaging Material Lab.
- To ensure availability of lab chemicals, lab stationaries and other lab related items in Central Quality Control, Stability, Microbiology Lab. and Packaging Lab.
- Preparation and review of Schedule/Planners (In-House Calibration, External Calibration, PPV-PTS and PPV-SPR).
- Preparation and maintenance of Calibration Standards/ Primary Standards as and when required.
- Ensure timely completion of Periodic calibration of laboratory instrument and its associated activities.
- Coordinate with concern stake holders and vendors for timely completion to GLP and instrumentation related activities.
- Document analytical data and calculate the results.
- Ensure integrity, accuracy and adequacy of the analysis/activity to be performed.
- Ensure accuracy of document and maintain neat/concise/organized analytical/activity data.
- Perform other activity as and when required.
- Ensure Compliance to cGMP requirements and laboratory procedures.
- Co-ordination with External vendor for calibration/Preventive maintenance activity whenever required.
- Responsible for ensuring cGMP and GDP compliance during routine work.
- Responsible for ensuring integrity, accuracy and adequacy of the activity performed.
- Accountable for all activities related to instruments, GLP, Qualification and Documentation.
- To ensure contamination controls implemented and followed at site as per Contamination Control Strategy (CCS) and respective procedures.