Bachelors or Masters degree in Pharmacy, Pharmaceutical Sciences. Lead and manage the technology transfer of pharmaceutical formulations from R&D to manufacturing Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs
Bachelors or Masters in Pharmacy. Must have exposure in handling of Process Area maintenance like Manufacturing Vassals, Filling machine, Autoclave, Isolators and Lyophilization.
M. Pharm / M. Sc / B. Pharm / B. Sc; Experience in Method Validations and Verifications, Analytical Method Transfers with Brazil Regulatory exposure. Experience in Finished Product, In-Process, Stability and GLP activities
M.Pharm; Analytical Method Validation. Development, Transfer activities. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule
A Post-graduate, Graduate degree in Chemistry, Pharmacy, Life Sciences. Candidate should have knowledge about Post-approval change submission requirement and compilation of variation packages for US, CAN, EU, AUS-NZ, ROW markets.
Bachelors degree in a scientific, health, communications, technology health related field. Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects.