vacancies

Operate equipment such as Granulation, Compression, Coating, Capsule Filling, Blister Packing, and Bottle Packing.

Process Validation / BPR / BMR/ Equipment Qualification / Audit & Compliance / Engineering & Compliance / Investigation Team

Should have hands on experience in Water samples analysis, In-process Bioburden and BET analysis, MLT analysis of Raw material and packing material, Antibiotic assay by Microbial method.

Having Injectable Experience of Shop floor activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions, filtration, Lyophilizes.

Review of analytical documents with relevant Raw Data, protocols, and Report Etc. Review of tending of the testing of Raw material, Finished Products, Stability samples & Raw materials

Ph.D/MD/MS/MDS or equivalent degree or having 03 years of research, teaching and design and development experience after MVSc/M.Pharm/ME/M.Tech with at least one research paper in long non-coding RNAs Journal.

M.Sc 1st Division or Ph.D in Chemistry/Bio-Chemistry /Toxicology/Forensic Science with Forensic Chemistry and Toxicology subjects or its equivalent qualification in any one of the above subjects/disciplines

B.S. 4 years program, B.Pharm., M.B.B.S., Integrated B.S.-M.S., M.Sc., B.E, B.Tech. or equivalent degree, with 55% marks and passing of NET-LS/GATE test.

First class Master Degree in any field of Pharmaceutical Sciences. GPAT or equivalent qualification. Experience in ophthalmic formulation development, Polymeric Patch- based drug delivery systems.