Cipla

Responsible for the coordination of supportive equipment and process validation activities such as testing, calibration, scale-up, engineering and validation studies, and assurance that the necessary project documentation is complete, accurate and in compliance with cGMP regulations.

Deviation and CAPA Support. Assist in documentation and tracking of deviations, change controls, and CAPAs. Participate in root cause analysis and follow-up actions.

Cipla walk in for candidates having Exposure in OSD Formulation Manufacturing. Candidates having experience in one of the following would be preferred Granulation, Compression, Coating, Hard Gelatin Capsules, Soft Gelatin Capsules and Pellets.

Should have sound knowledge of BFS machine operation, aseptic area, maintenance, media fill, batch mfg, CIP, SIP, Autoclave.

M.Sc. / B. Pharma. Experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms.

The purpose of the QA Manufacturing Inspector position is to monitor and ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures.

Operate & maintain packing machines to achieve quality product & shift wise targeted output with maximum utilisation.

Perform part method validation, forced degradation studies, excipient compatibility studies, reverse engineering, add-mixture studies, in-use studies, hold-time study and analysis of routine & stability studies

Graduate in Pharmacy or Life Sciences. 2 years in the field of Regulatory Affairs/ Quality Assurance/ Quality control/ Manufacturing/ Analytical Development/ R&D.