5+

Handle manufacturing skids, Fedegari autoclaves, Isolator lyophilizers, vial washing and tunnel, vial, ophthalmic ,PFS filling and aseptic filtration, FFS, CIP,SIP, filters, microsphere refiner, Active freeze drying System. Operation, cleaning, sterilization, qualification and maintenance of solution preparation systems.

Lead active surveillance and analysis of emerging regulations, perform impact assessments and drive process changes required to ensure ongoing compliance to global regulatory requirements. Analyze the impact of other Novartis processes and organizational changes on assigned processes.

Online filling of the BPRs and records and performing jobs related to SAP, Operate equipment's reactor, Sparkler Filter, Candle Filters , Centrifuge, Dryers as per SOP

Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates.

Bachelors, Master degree or PhD in science, math, engineering or related discipline; The Principal, Regulatory Affairs, Intelligence, Materials is expected to perform with minimal supervision and is an experienced and detail-oriented professional with expertise in materials and with an understanding of the interplay of materials and medical devices, pharmaceuticals and combination products.

M.Pharm / M.Sc. jobs; Analysis of Finished product, Method development, validation, Documentation as per GLP Stability analysis of finished products, calibration of instruments

Assists Head-Bioanalytical in the smooth running of the bioanalytical section through efficient project and quality management in conformance to GLP guidelines.

B.Pharma, M.Pharma - IPQA; B.Tech, B.E Any stream in Nutraceuticals, Chemical, Pharma devices, Pharma equipments, FMCG, API, Packaging.