Masters degree in Biotechnology, Microbiology, Biochemistry with a qualified National Eligibility Test–CSIR-UGC-NET, LS or DBT-BET, ICMR, Fellowship, JEST, JGEEBILS or GATE.
Demonstrated understanding of pharmaceutical manufacturing, analytical testing, and quality assurance. managing CMC Regulatory submissions for small molecules/vaccines/biologics
M.Sc. in a relevant field such as Biotechnology, Biochemistry, Life Sciences or a related discipline. Basic laboratory skills acquired through academic course work, internships, and research projects.
M.Sc Botany, Zoology, Biochemistry, Applied Biology, Life Sciences, Biotechnology, Microbiology OR M.Tech Biotechnology, Life Sciences with minimum 60% marks and with a Diploma in Medical Laboratory Technology from a recognized institute.
Ph.D. in Environmental Engineering, Biotechnology, Microbiology, Chemical Engg, Climate Change or other allied areas.
Experience with handling chromatography instruments preferred.