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● 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
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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