Responsible for managing QA documentation, ensuring GMP compliance, and supporting quality systems through effective handling of SOPs, BMR/BECR review, validation and qualification activities. Oversees document control, vendor qualification, calibration and maintenance coordination, and ensures timely closure of deviations, change controls, and CAPAs while maintaining data integrity and audit readiness across all QA operations.
Issuance, archival and retrieval of documents.
Issuance of Control coples to respective dept.
Destruction of the GMP documents once the retention term has passed and controlled coples of the obsolete GMP documents.
Tracking of all QA documents. 5. Maintaining backup of QA softcoples.
Maintaining SOP/s with proper indexing.
Preparation and review of SOPs
Management of QA Stationary (Controlled Coples and logbooks)