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.
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.
First Class in Masters / M.Pharm / M.Sc. in Pharmacology / Biochemistry / Pharmaceutical Sciences / Sports Sciences from recognized University / College / Institutes with relevant experience in scientific research / technical administration / management.
M.Tech. / MD / MVSc / M.Pharm / M.Biotech with R&D experience. OR Ph.D or corresponding degrees in other disciplines with original work as evidenced by patents or publications.