Masters degree in Biotechnology, Virology, Biochemistry, Microbiology or any equivalent field with minimum 55% marks and must have qualified NET or GATE.
M.Sc in Life Science / Biotechnology / Microbiology /Genetics / Biochemistry / Zoology / Genomics with minimum aggregate 60% marks or M.Tech (Biotechnology / Life Sciences) with minimum aggregate 60 % marks.
Oversee the timely order and shipment of comparative samples from various suppliers to partners and Clinical Research Centres (CROs) globally to assist in bioequivalence studies.
Responsible for release of the product by ensuring review of relevant audit trial of Manufacturing. Strong knowledge of cGMP, ICH guidelines, FDA regulations, and other relevant standards for biologics manufacturing.