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Centaur Pharmaceuticals one of the rapidly growing Pharmaceuticals Company in India. Centaur Pharmaceuticals is USFDA and MHRA approved plant is seeking deserving candidates having experience working in Oral Solid Dosage Manufacturing facilities for regulatory market's.

Plan, execute & ensure timely submission of various applications when assigned including but not limited to only these: test license application, HAQ response submission, CT updates and notification submission e.g. IB amendment, site closure, site addition, EC approval submission etc.

The ideal candidate will have advanced Excel skills and a background in Pharmacovigilance and Safety Operations or Research and Development. This hybrid role requires rotational shifts and offers an opportunity to make a significant impact on our projects and society.

Must have worked in regulated plants having approvals of USFDA, MHRA. etc. Hands-on experience in handling and implementing cGMP Current Good Manufacturing Practice practices and Good Documentation Practices

Candidate should have experience in Oral formulations Solid and liquid for Handling of IPQA, APQR activity and Process Validation. Candidates must have experience in review of Analytical Document, Investigating out-of-specification results, and ensuring adherence to GMP guidelines.

Achieve Division wise primary target and ensure it to be equal to or greater than Secondary. Generate maximum prescriptions & increase market share. Ensure zero cases of expiry on Stockist shelf by timely liquidation of stocks by prescription generation.

Sun Pharmaceutical Medicare Limited is taking this opportunity to balance employment and the medications for the world. Batch Manufacturing Record, BMR Requisition, BMR Issuance Logbook.

To create specialized content with supervision; support end-to-end publication, medical education content development process including documentation and approval in PromoMats, iEnvision; develop and maintain therapeutic area expertise; work in close collaboration with peers, team to develop best practices; and collaborate effectively with stakeholders.

B.Pharm, M.Pharm, M.Sc, B.E. with 2 to 10 Years of relevant experience of IPQA, Qualification, QMS, Sterility Assurance, QA IT related activities in Injectable Manufacturing Plant.