Description
Key Responsibilities:
- Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility.
- Responsible for preparation and review of protocols and reports based on the requirements.
- Responsible for document management and preparation like BMR’s, BPR’s, master SOP’s etc.
- Responsible for the handling of change control, deviations, CAPA, investigation etc.
- Responsible to give training to all the subordinates, technicians and operators of the department.
- Responsible for Audit and compliance on manufacturing shopfloor.
- Knowledge of kaizen and continuous improvements.
Qualifications
Qualification: B.Pharm/M.Pharm
Experience: minimum 2-5 years experience in manufacturing QMS/Process review/Compliance.