Scientist Pharmaceutical Development at Aurigene. Plan and execute pre-formulation studies, stability studies etc for mAB and ADC projects during early stages of pre-clinical development.
BTech / Masters in Technology or Masters in Business Administration. The Execution QA comprehensively reviews rendering quality, Metadata, Content Matrices. Novartis
Strong background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems. Ability to work both independently and collaboratively.
Having Injectable Experience of Shop floor supervising activities like filtration, Filling, Sealing, Stoppering, Garment Washing, Vial Washing, Autoclave, Ophthalmic, Suspensions, Lyophilizes. Operations and Training and QMS.
Regulatory Affairs Executive is responsible contribute regulatory expertise in various aspects including regulatory submissions, right first-time dossiers, timely addressal of queries, etc. for various product categories such as Cosmetics, Commodities etc.