To ensure cGMP compliance at the shop floor for Drug Substance (DS) manufacturing through effective line clearance, documentation review, in-process oversight, and quality systems activities.
QA professional experienced in GMP documentation review, process and cleaning validation, QMS management (Change Control, Deviation/Event, CAPA), analytical data review, SOP management, and regulatory compliance activities.
Operate assigned production and packing machines as per approved SOPs and work instructions. Perform machine start-up, operation, adjustment, and shutdown activities as per established procedures. Piramal Pharma Solutions