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Posted:Invalid date| Platform: 
Work from Office
Full Time
Preparation and review of SOPs, BMR/BPR. To process Change control and Deviations. Proficient in handling Track wise To initiate Change Control, CAPA, Deviation, Risk assessment, Market complaint, Investigation To update and maintain Index of SOPs and Formats. To issue & Retrieve Logbooks, Formats etc. To assist in compliance for internal and external audits On line training module knowledge. Should have good knowledge & proficiency in Computer. Must have worked in QMS of reputed Pharmaceutical industry Awareness of internal and external audit dealing is required Regulatory plant experience
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