Exposure of analysis for Finished Products, Stability Samples and Raw Materials. Having Knowledge of Analytical Method Validation, Verification & Method Transfer.
Review of Master Batch production and control record BPCR and review of Master media fill records & Review of complete Batch records before release. Preparation and review of media fill Protocols and Reports.
B.Pharmacy, M. Pharmacy, M. Sc.,B.Sc., Diploma with relevant functional experience in injectable manufacturing, Aseptic area operations, Packing, Visual inspection, QMS activities
Full Time Bachelors degree in Pharmacy with State Pharmacy Council registration and Post-Graduate Degree, Diploma in Material Management, Business Administration from reputed institute
B. Pharm , M.Sc. , M. Pharm with 2-8 years of relevant experience in IPQA , validation , Documentation related activities in Oral Solid,Oral Liquid,Semi Solid dosages manufacturing facilities.