SUN PHARMA
Job Summary
- Responsible all Activity related to GLP, raw material, packaging material.
Essential Job Functions
- Planning & work allotment for RM, GLP and packaging materials.
- Review the Raw material data and packing Material data and release.
- Assist in developing and updating SOPs, work instructions, forms, etc.
- To Review stability data in Stability system.
- To release the packaging, raw material and finish product.
- Change Control/Deviation/CAPA management w.r.t. quality control activity and ensure timely closure.
- Preparation & Review of Specification / STP and SOPs of respective work area.
- Monitoring of gowning and sanitation practices in area of operation.
- Monitoring of compliance of standard operation procedure for operation of analytical instrument.
- To follow the procedure of good documentation and recording of result as per SOP on GDP and good execution of laboratories practices.
- To support the internal audit/Regulatory/FDA audit with best of practices
- Following all regulations of cGMPs as per schedule M.
- To maintain the safety procedure in handling analytical equipment and hazards
- Completing the training assigned as per the training need identified by participating in trainings organized or self-reading.
- To calibrate the analytical equipment’s as per the calibration procedure for assigned responsibility of calibration.
- To maintain the analytical equipment’s and laboratories in good state of operation.
- To follow procedure for non-conforming result as it is applicable in SOP of OOT, OOS and Lab Incident.
- To follow the administrative procedure of compliance with respect to term and condition for attendance, leave and other benefits.
- To ensure training of reporting employees and related documentation on time.
- Responsible for work assigned by Head QC.