Centaur Pharmaceuticals Pvt.Ltd.
Urgently Required We are one of the rapidly growing Pharmaceutical Company in India. Centaur’s USFDA & MHRA approved plant in Pune is seeking deserving candidates, having experience in Formulation /Oral solid dosage and regulated markets.
QC Officer/ Executive Candidates should be M.Sc. (Chemistry) with 4 to 6 years of experience in QC in Formulations regulated manufacturing company. Experience must include analysis of Finished goods (Tablets / Capsules), handling HPLC, dissolution & other sophisticated instruments. Exposure to regulatory audits like USFDA, MHRAis mandatory.
QA Executive – QMS Candidates should be B.Pharm/M.Pharm with 4 to 8 years of experience in QA in Formulations regulated Manufacturing Company. QA activities would include Documentation, Validation, Internal & External Audit, Master Documentation Creation, Handling customer complaints, CAPA, Vendor management, OOS, OOT, analytical data review. Candidate should be well aware of data integrity concept, GLP Practices. Exposure to regulatory audits like USFDA, MHRA, is must.
Asst. Manager-QA(QMS) Candidates should be B.Pharm/M.Pharm/M.Sc with 8 to 12 years of experience in Formulation Regulated Manufacturing Company Candidate must have exposure to handle QMS system, Design, Preparation, Review, Approval and Implementation of quality system related standard operating procedures (SOPs) & document, Management of complaints & failure investigations Management of LER, OOS and Out of Calibrations (OOC), To conduct Training on CGMP and other Quality aspects, Vendor management for raw materials & packaging materials, Review of trending of OOS, OOT, OOE, deviations, incidences, CAPA and Change Control, Allocation of work, roles, Responsibility and Authorities of QMS Department.
Asst. Manager RA Candidates should be B.Pharm/M.Pharm with 8 to 12 years of experience in formulation regulated manufacturing company. Candidate must have experience in Submission of application/Dossier/ANDA, Regulatory Queries, Compilation of Dossier, Assures compliance with respect to regulatory requirements, Dossier preparation for Technology Transfer / site Variation / New development products, Co-ordinate with client representatives for project updates
Interested candidates may send their application along with CV addressed to firstname.lastname@example.org , Ph-020 6673 9510/509