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.
Subject Matter Expert for Drug-Device Combination Products will serve as a key resource within the organization for technical expertise and regulatory guidance related to the development, manufacturing, and commercialization of drug-device combination products.
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.
Bachelors or Masters in Pharmacy. Must have exposure in handling of Process Area maintenance like Manufacturing Vassals, Filling machine, Autoclave, Isolators and Lyophilization.
VBPL is an ISO 13485:2012 and WHO – GMP certified leading global player in Biopharma sector having more than 15 years of operational experience, situated at Hyderabad. We also have offices located in USA. Innovative, ever motivated Research team and uncompromising manufacturing team in providing quality products are our strengths.