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Centrient Pharmaceuticals Netherlands | Rupnagar, India | Posted June 09, 2026
Position Overview
To ensure that the Products provided to the market are tested as per Customer specifications and in compliance with applicable pharmacopoeias as well cGMP/GLP/ICH/USFDA /ISO guidelines.
Key Responsibilities:
To participate in vendor qualification activities. To participate in Internal/External audit activities To ensure compliance as per applicable regulatory requirement. Release/rejection of finished products, intermediates & raw material as per approval specification Creation & release of Certificate of analysis. Issuance and review of Batch production records. QC analytical data review. Handling sales return, recalls and compilation of APR data To coordinate investigation of market complaints/deviation/OOS/OOT. Log books management for various activities. To ensure that sampling of all Finished products are done as per defined procedure and proper r...