Develop, maintain, and update laboratory systems and documentation, including SOPs, IQ/OQ/PQ documents, training records, and related quality documents.
USV Private Limited is a prominent Indian multinational pharmaceutical and biotechnology company founded in 1961, specializing in diabetes and cardiovascular therapeutics
To facilitate the Change Controls to be logged for various reasons. To initiate the Change Controls due to revision in BMR / BPRs and other PD related changes
M.Pharm, B.Pharm, M.Sc, B.Sc. Responsibility of Quality Control Laboratory Planning and co-ordination. Supporting timely release of samples as per production plan. Co-ordinating with PPIC team for daily manufacturing activities against the QC planning.
Must have worked in regulated plants having approvals of USFDA, MHRA. etc. Hands-on experience in handling and implementing cGMP Current Good Manufacturing Practice practices and Good Documentation Practices