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.
Working in partnership with the Client Engagement team, Medical Communications, and the Writing delivery team for a designated client group/therapeutic area (TA) / brand, this role will be responsible for delivering and supporting scientific excellence of Medical Communications services across their accounts
The incumbent will support the formulation development team for development of cosmetics and commodity products. Work collaboratively with internal and external stakeholders to meet the development timelines.
Responsible for regulatory activities specifically related to chemistry, manufacturing, and control (CMC). Activities such as the preparation and publication of REG CMC documentation for submissions to Health Authorities.