Review of BPR, batch cleaning record, test data sheet, Sampling of API finished goods. Preparation of APQR. Handing of QMS document Change control, Deviation, CAPA, OOS, OOT review.
Master Degree in Chemistry, Organic Chemistry, Medicinal Chemistry from a recognized University or equivalent. Hands-on experience in multistep small to large-scale organic synthesis.
Ph.D. in Biotechnology, Life Sciences, chemistry, physics from a recognized University, Institute. Minimum Two years post-doctoral experience in Microscopy or Flow Cytometry.
M.D Pharmacology M.V.Sc. Pharmacology M.Pharma, M.Sc. Medicinal Plants with specialization in Pharmacology from a recognized University Institution. Post Graduate degree in the Chemistry from a recognized University, Institution.
Antiviral Mission: CSIR Discovery and Pre-clinical Development of Antivirals for COVID-19 and other diseases. reclinical Pharmaceutics and pharmacokinetic studies of CDRI candidate drugs, formulations and phytopharmaceuticals. M.Pharm. with GPAT qualified. Master in Chemistry, Chemical Sciences, Pharmaceutical Chemistry.
Candidate should have knowledge of manufacturing operations of granulation, compression, coating and capsule filling, responsible to adherence cGMP guidelines. USFDA, MHRA exposure is must.
BTech, MTech in Biotechnology, Biomedical Engineering, Mechanical Engineering, Chemical Engineering, Polymer Engineering, Materials Engineering or relevant discipline; M.Pharm, MS in Pharmacy, or MSc in Biotechnology, Biochemistry, Zoology, Microbiology, Chemistry