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.
Masters with PhD from a recognized University in Pharma, Chemistry, Biochemistry, Biotechnology candidates. Indian Council of Medical Research, ICMR. Experience in Maternal, Child Health and Nutrition
Proven research experience in the area of Metabolic engineering or Synthetic Biology. Demonstrable expertise in genome engineering of microorganisms as evidenced by original research publications in SCI journals and/or granted patents. Institute of Microbial Technology
Ph.D. in Health Sciences with first class or equivalent grade at the preceding degree (M.Pharm./M.S./M.Sc./M.D.) in Pharmacy Practice, Clinical Pharmacy, Clinical Pharmacology
Responsible for safety monitoring and evaluation of assigned GSK products. Conduct safety monitoring and evaluation for assigned products, including signal detection and risk assessment.
Masters Degree in Biotechnology/ Agricultural Sciences/ Natural Sciences or Bachelors Degree in Engineering or Technology with specialization in Biotechnology/ Microbiology/ Molecular Biology from a recognized University or equivalent
Responsible for discussion and planning strategies for product development, executing them and recording them in E-Lab notebook. Identify and proactively discuss potential challenges along with possible way forward.
M.Pharm./MS.Pharm. Pharmaceutical Analysis / Quality Assurance / Natural Products/ Medicinal Chemistry or Post graduation in M.Sc. Analytical Chemistry/ Organic Chemistry, National Institute of Pharmaceutical Education and Research.