Experience in analysis in HPLC / GC, Qualification / Re-Quaiification of Laboratory instrument(DQ/IQ/OQ/PQ), Preparation of AMV protocol. Responsible for QMS activity like : CCP, Deviation, OOS, OOT, UR.
Openings in R&D, AR&D, Production, Labelling & Packing at Hetero Biopharma. Process development & scale-up. Tech transfer experience. DoE / QbD based process studies
Operate & manage granulation, compression, coating, pelletization and capsule filling area. Operate and monitor pharmaceutical manufacturing equipment as per SOPs, BMRs, and GMP guidelines.
A Post-graduate / Graduate degree in Chemistry / Pharmacy / Life Sciences or others. Candidate should have understanding of various departments in pharmaceutical company.
Experience in pharma industry for handling shift-related activities like work schedule, release of in-process and intermediate samples etc. Natco Pharma