Centaurs USFDA and MHRA approved plant is seeking deserving candidates having experience working in Oral Solid Dosage Manufacturing facilities for regulatory markets.
B.Pharm / M.Pharm. Responsible for Review of the batch manufacturing Record & Line clearance for OSD Area. Monitoring packing stability Batches, Zenotech
Perform QA audits internally and at investigator sites of clinical trial data & records to assure compliance with SOPs, study protocols. Good Clinical Practice Guidelines and relevant regulations.
M.Pharm, B.Pharm, M.Sc, B.Sc Candidates must be open to work in shift duties and having pharma experience in regulated plant like USFDA, MHRA should apply.