MSc / PhD degree in life sciences with experience in handling human clinical samples, biochemical assays, flow cytometry, FlowJo analysis, and cell-based assays.
PG degree including integrated PG degree such as M.S. Pharm/ M.Pharm/ M.Sc/ M.Tech or Equivalent with specialization in Pharmacology and Toxicology/ Regulatory Toxicology/ Pharmacoinformatics/ Biotechnology/ Life Sciences
Postgraduate in the field of Life Sciences or Pharmaceutical Sciences or any other allied Life sciences; National Institute of Pharmaceutical Education and Research
PHARMACY GRADUATE WITH 3 TO 7 YEARS OF EXPERIENCE IN FORMULATION DEVELOPMENT OF STERILE DOSAGE FORMS AS PER GUIDELINES OF US, EU, CANADA, BRAZIL AND ROW MARKET.
First-class PG degree, including integrated PG degree. Candidates with hands-on experience in, Recombinant DNA Technology, Bioprocess Engineering, Metabolic Engineering and Mammalian cell culture-related work will be preferred.