B.Pharm

Analysis and processing of In process and Finished product and handling of HPLC, UV, FTIR, K/F, AAS, IC, Dissolution. Analysis of Raw material and Excipients and handling of HPLC.

After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.

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.

Bharat Technology is a premier college in Howrah, West Bengal with 19 years of academic excellence. Presently we are conducting fulltime Pharmacy courses like M.Pharm., B.Pharm and D.Pharm.

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

Execute Analytical method Validation activities of drug substances API by using HPLC,GC and Spectroscopic techniques as per regulatory guidelines. Execution and coordination for Analytical method transfer activities of drug substances.

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.