We are looking for a detail-orientented Quality Executive to manage and maintain accurate batch manufacturing records and ensure compliance with regulatory standards. The candidate will be responsible for documentation, record verification, and audit readiness in a medical/pharmaceutical manufacturing environment.
Key Responsibilities
Maintain and update Batch Manufacturing Records (BMR) accurately
Ensure compliance with GDP (Good Documentation Practices) and GMP guidelines
Prepare, review, and manage Standard Operating Procedures (SOPs)
Verify batch records for completeness and accuracy
Document and report deviations, incidents, and discrepancies
Ensure all records are audit-ready and properly filed
Coordinate with production and quality teams for documentation support
Maintain proper version control and documentation traceability