Masters in Life Sciences. Participate, as needed, on global teams to complete assignments and tasks within a specific task force/project associated with labelling
Responsible for analytical method development, analytical method validation, stability study, method transfer and other end to end projects analytical activities. Responsible for assigned lab compliance activities.
M.Sc, M.Tech, M.Pharm in Life, Biological, Allied life Sciences, Pharmacy. NET-JRF or LS, GATE qualified Two years experience in research and development in academic,industrial institutions
Routine cell culture, differentiation of cells, transfection of cells, gene editing by CRISPR, Cas9, lentivirus preparation and transduction, analysis by western blotting, qPCR, ChIP, microscopy and various biochemical kits
Masters Degree in Pharmacology, Drug Assay, Chemistry,Biochemistry, Zoology, M.Pharma Ay, MSc Medicinal Plants with specialization in Pharmacology from a recognized University, Institute
Regulatory Affairs Manager in the Regulatory Business Development Post Deal Management group is a regulatory specialist with project management capabilities responsible for both regulatory life cycle maintenance submissions and managing successful application transitions for products that are either divested or acquired.
Syngene International Limited is hiring for Compound Management division post M.Pharm, M.Tech, M.Sc, B.Pharm, B.tech, one-of-a-kind facility in India, comprising fully automated solid and liquid storage, integrated acoustic dispensers and liquid handlers.