First class Post Graduate Degree in Biotechnology / Biochemistry or in related fields of Biological Sciences, including the integrated PG Degrees, with three years experience in Human iPSC culture and differentiation / human embryonic stem cell culture.
M.Pharm / M.Sc. (Biotechnology) / M.Tech (Nanotechnology or Biotechnology). Qualification in a national-level competitive examination such as CSIR-UGC NET, GATE, or equivalent.
First Class Post Graduate Degree, including the integrated PG degrees with three Years of relevant Experience or Ph.D. OR Second Class Post Graduate Degree, including the integrated PG degrees with Ph.D. and three Years Experience.
Responsible for ensuring cGMP compliance in the QC laboratory, reviewing analytical documentation, and approving Certificates of Analysis for all materials and products.
Masters degree in Pharmacy or Clinical research. Plan and perform vendor qualification and audits for pre-clinical, clinical, and In-vitro studies service providers.
Masters in Pharmacy or Masters in Science / Life Sciences. College or University degree or equivalent work experience that provide knowledge of and exposure to fundamental theories, principles and concepts.