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
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,
● Department: Quality Assurance and Regulatory Affairs ● Reports to: QARA Manager ● Experience: 3 to 5 years in medical devices ● Location: Hybrid– (BTM Layout, Bangalore) ● Qualification: Bachelor’s degree in engineering, sciences or Pharma