Masters Degree in Pharmaceutical Sciences First-class with GPAT qualification Preferably in Pharmaceutics from a recognized University. GATE, NET, GPAT qualification with prior experience working on a project related to developing nanoformulations, mammalian cell cultures, and in vivo experiments. Strong interest in learning new techniques Proficiency in spoken and written English is highly desirable.
Review of Master Batch production and control record BPCR and review of Master media fill records & Review of complete Batch records before release. Preparation and review of media fill Protocols and Reports.
Subject Matter Expert for Drug-Device Combination Products will serve as a key resource within the organization for technical expertise and regulatory guidance related to the development, manufacturing, and commercialization of drug-device combination products.
Routine cell culture, differentiation of cells, transfection of cells, gene editing by CRISPR, Cas9, lentivirus preparation and transduction, analysis by western blotting, qPCR, ChIP, microscopy and various biochemical kits
MSc, M.Tech, M.Pharm. in relevant stream of Biological Sciences with 3-5 years of relevant experience in Analytical R&D, QC department of Biopharmaceutical industry.
BS, RN, MS, PharmD in life sciences or equivalent relevant scientific qualifications or professional training. Generate and file data for signal detection and safety data review. Demonstrated understanding of global pharmaceutical drug development and lifecycles.
Overcoming the Inflammatory Cascade in Neonatal Sepsis, a Nanomedicine Approach. First class post-graduate PG degree including integrated PG degree such as M.S. Pharm, M.Pharm, M.Sc, M.Tech or Equivalent with specialization in Pharmacology & Toxicology, Regulatory Toxicology, Biotechnology, Life Sciences.