Job Description

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.

Sun Pharmaceutical Industries