Officer, IPQA
IndiaFull-time2–5 yrsPosted over a month ago
Mid-level pharma role at Hcfa. Needs 2+ years and a B.Pharm or M.Pharm.
About the role
1 cGMP and compliance review in the GMP area as per cGMP guideline. 3 Sampling of blend, intermediate stages, AQL finished product, ANSI sample, reserve sample, stability sample and In-process checks during execution of batch manufacturing & Packaging as per Process Study Protocol (PSP), Process Validation Protocol (PVP), Batch Manufacturing Record (BMR), Batch Packaging Record (BPR) & miscellaneous protocol based study.
What you need
- GMP
- Calibration