M.Sc. in the field of Biology, Molecular Biology, Human Genetics, Cell Biology, Biochemistry, Microbiology. Candidates with UGC-CSIR / NET / GATE / ICMR-JRF / DBT-BET qualifications will be preferred.
Knowledge of global and regional pharmacovigilance regulations. Experience in Pharmacovigilance, data management, and adverse event reporting and processing, with proficiency in relevant software tools.
Design, execute, develop, and optimize upstream process for biosimilars monoclonal antibodies, fusion proteins in CHO Cells. R&D USP Mammalian, R&D Analytical, R&D Bioassay
Bachelor degree in Pharma or Life Science. pharmaceutical sales experience, preferably with diabetes products. Consistent record of meeting or exceeding sales targets
Facilitate and manage corporate quality audits and regulatory audits and drive the Supplier Qualification Program, including the identification, evaluation through audits, monitoring, maintenance, and re-qualification of vendors.