Officer

18 hours ago

Baddi, India Sun Pharmaceutical Industries Ltd Full time

**Title**:Officer**:

- Date: Apr 25, 2025
- Location: Baddi - Quality Assurance
- Company: Sun Pharmaceutical Industries Ltd
- Monitoring of gowning and sanitation practices in area of operation.
- Monitoring of compliance of standard operation procedure in production & packaging department.
- Reporting the noncompliance of written SOP of machine operation.
- Line clearance inspection and clearance of cleaned area, Equipment on compliance with checklist, reporting of noncompliance to area supervisor and QA Executive.
- In process testing-sampling and performing in process test of Running Batch in area of Supervisions per defined frequency.
- Sampling-performing sampling of blend/Bulk, in process validation/stability samples and finished good as per standard operating procedure and submitting sample to concerned lab instantly. Maintain sample receipt log for the same.
- Reporting shift activity in log as per SOP.
- Verifying critical process parameter as defined in Batch Process record (MI & PI).
- Reporting deviation process breakdown in shift report.
- Verifying stage wise yield.
- Verifying on time entries by Production workmen & Staff.
- Reporting any abnormal environmental condition Temperature % RH, differential pressure difference to shift supervisor for rectification, if problem persists initiating deviation.
- Completing the training assigned as per the training need identified by participating in trainings organized or self-reading.
- Investigating reported market complaint, deviation OOS.
- Following all regulations of cGMPs as per schedule M.
- To support the internal audit/Regulatory/FDA audit with best of practices.
- To operate the analytical equipments in Q.C. as per the allotted work in the shift.
- To calibrate the analytical equipments as per the calibration procedure for assigned responsibility of calibration.
- To follow the procedure of good documentation and recording of result as per SOP on GDP and good execution of laboratories practices.
- To report the observations of analysis on analytical equipments promptly in respective BPR’S.
- To maintain the analytical equipments and laboratories in good state of operation.
- To maintain the safety procedure in handling analytical equipment and hazards.
- Completing Batch Process record entries in shift.
- Following all standard operating procedure applied to IPQA & Plant Procedure

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