To ensure finished products are release in timely fashion through reviewing and checking completion batch manufacturing record.
To ensure that the manufacturing document e.g. BMR for products are maintained and updated with the latest requirement / amendment by monitoring/initiating the change control and deviation.
To ensure all documentation, SOP and other GMP related records are in order and update manner.
To ensure Certificate of Analysis (CoA) for each batch produced is available for shipment and registration purpose.
To coordinate and monitor Rework, Redress and any Rejection activity.
To ensure appropriate handling and filing of Quality related reports e.g. Inventory Request (IR), Item Master etc.
To participate actively in self-inspection programs organized by QA department.
To cover the responsibilities of other QA Executives in their absent.