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Syngene is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.

Hands on Experience for handling critical lab instruments like HPLC, GC, Dissolution, UV Spectrophotometer, LIMS, FTIR , experience in Analysis of RM, FP and IP stability in QC.

Candidate must have 2-7 years of experience in production, including operations and supervision of autoclave processes terminal sterilization and components, filter integrity testing, aseptic and controlled area operations, as well as proficiency in vial washing and filling machine operations.

Manage R&D development related research for specific Drug Delivery Systems to ensure on-time, within budget quality delivery along with a continuous focus on improvements. The candidate will be responsible for conducting hypothesis testing, designing and developing novel formulations using various materials for diverse applications, including development of Liposomal formulations, Nano- and submicron particulate formulations, Polymeric-Based Formulations, etc.

M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma. 2-6 years of experience in operating of Granulation, Compression, Packing.

Finished, AMV & Stability Section, knowledge of Instrument - HPLC, GC, Preferably know-how of Chromeleon Software.  Good exposure require in IPQA - OSD & Sterile, Qualification OSD & Sterile & Documentation Cell

2-6 years of exp. in Finished Goods, Raw Material, Packing material, Stability and GLP. 2-5 years of exp. in AQA, Documentation.

Finecure Pharmaceuticals Limited and its subsidiaries are leading manufacturers and marketers of Pharmaceutical formulations and Nutraceuticals in several therapeutic segments in dosage forms of Tablets, Capsules, Oral Liquids, Dry Syrup, Powders, Injections and Sachet.

M.Pharm/ B.Pharm/ M.Sc/ B.Sc; experience in production including operation and supervision of autoclave operation TS and component, Filter integrity, aseptic & control area operation, vial washing and filling machine operation. Injectable /parenteral/sterile manufacturing experience is a must. experience in bulk manufacturing/aseptic filling, control/aseptic area operation, vessel operation including CIP/ SIP process handling, machine operation Steam Sterilizer, Vial Washing, and GMP documentation.