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Key Responsibilities Lead overall Quality Assurance and Quality Management System (QMS) activities in compliance with cGMP and regulatory requirements. Review and approve SOPs, BMR/BPR, specifications, validation/qualification documents, SMF, VMP and other quality documents. Manage OOS/OOT, deviations,
GMP Compliance – Drug Product Facility Monitor day-to-day activities and plan allocation of IPQA personnel as per batch schedule. Oversee critical manufacturing activities including dispensing, in-process checks, sampling, filling, sealing, visual inspection, and AQL. Coordinate with Drug
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