Centaur Pharma

Knowledge of QC instruments & handling of trouble shooting of critical Instruments. Defining departmental employee roles, responsibilities and authorities. To monitor upkeep and compliance of laboratory in regulatory view.

Candidates should have experience in Formulations regulated manufacturing company such as USFDA and MHRA, EU. Exposure to regulatory audits like USFDA, MHRA, EU is mandatory

Experience must include analysis of Raw Material, In-Process, finished goods; Stability Testing & Stability sample handling for Tablets, Capsules Handling of HPLC, dissolution & other sophisticated instruments.

Centaur Pharmaceutical is the largest specialty of drug manufacturing Organization. We provide high quality affordable medicines trusted by healthcare professionals like USFDA and MHRA.

Knowledge of regulatory guidelines applicable to formulation development. Must have handled ER, MR, Pellets drug products for US and EU market.

M.Pharm. QMS/AQA/IPQA/ Validation/Documentation. Candidates should have experience in Formulations regulated manufacturing company such as USFDA & MHRA. Exposure to regulatory audits like USFDA, MHRA is mandatory

Centaur Pharmaceutical is the largest specialty of drug manufacturing Organization. We provide high quality affordable medicines trusted by healthcare professionals like USFDA and MHRA.

M.Pharm, B.Pharm, M.Sc; RM, Stability, In-process, FG, AMV and AMT, QMS, AQA, IPQA, Validation

To arrange RM/PM at location as per Production Plan and Safety stocks. To update critical product status on weekly basis. Update Export order status with RM & PM shortages and action plan for delayed order.