Responsible for reviewing batch manufacturing, monitoring process steps, and reviewing documentation. Additionally, support in handling deviations, change control, and CAPA management, internal and external audits to maintain compliance.
Msc (Life science) / B. Pharmacy / Diploma, M. Tech Biotechnology. Production - Bulk Manufacturing Drug Substance / Antigens , Production Formulations Injectables, Quality Control Biologics / Vaccines, QA
D.Pharm, B.Pharm, M.Pharm ; Handling of activities like granulation, compression,coating, SCADA based equipment and QMS, which includes CCR's deviations, market complaints etc.