Posted:2 months ago| Platform:
Work from Office
Full Time
Role & responsibilities Issuance, archival and retrieval of documents Issuance of Control copies to respective dept Destruction of the GMP documents once the retention term has passed and controlled copies of the obsolete GMP documents. Tracking of all QA documents. Maintaining of backup of QA softcopies. Maintaining SOP/s with proper indexing. Preparation and review of SOPs. Management of QA stationary (controlled copies and logbooks) Dispatch and line clearance activities. Review of BMR/BECR Involving in handling of deviations, change control and related CAPAs To ensure data integrity compliances while performing activities.
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