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5.0 - 9.0 years
0 Lacs
ahmedabad, gujarat
On-site
As a member of the Central Quality department, your role involves: - Conducting Vendor Audit & Compliances - Reviewing Procurement bill of material (PBOM) - Initiating and evaluating change control, Corrective and Preventive Actions (CAPA) through track wise software - Evaluating Certificate of Suitability (CEP) updation, Drug Master File (DMF) notification, and Vendor notification for implementation at formulation sites - Reviewing Quality Management System (QMS) documents of all sites - Auditing formulation sites as per self-inspection plan - Preparing Audit planner for Active Pharmaceuticals Ingredients, Excipients, packing materials, Key Starting Materials (KSM)/Intermediates, Sterile ar...
Posted 1 month ago
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