Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50
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
● 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