Posted:2 months ago|
Platform:
Work from Office
Full Time
Candidate should have Pharma API company background Handling And Responsibility Of QMS Documents Change Control Deviation Out of Specification Market Complaint Corrective and Preventive Action (CAPA) Document Controls All document Issuance & Retrieval COA preparation BMR & BPR Preparation & Review Specification, Method of Analysis & Protocol & Report preparation for Finished product, Intermediate product, In-process, Raw material, Packing material. Standard Operating Procedure (SOP) Preparation Customer Query Related work/investigation. Policies & system procedures preparation. Training Calendar preparation and control. Qualification / Calibration / Validation Responsible for all Calibration activity Internal & External and maintained the record. Responsible for Equipment Qualification & Documentation control Vendor Qualification and regular follow up for updated documentation by the supplier Perks and benefits Transportation Leave enashment Health Insurance
Redox Scientific
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