Quality Associate Iii
CurrentQA Associate III- Nightshift Works with manufacturing staff on the production floor to ensure all work is documented per cGMP requirements and standard operation procedures are followed. Helps manufacturing staff correct errors in cGMP documentation. Reviews and approves production documents including batch records, logbooks, and standard operating procedures. Reviews and approves Maintenance Work Orders, Testing Work Order, Calibration Work Orders in BMRAM. Also perform asset approval in BMRAM. Initiates and approves deviations. Organizes and leads meetings with multiple departments to determine the impact of a deviation on quality, patient safety, validation, and data integrity after deviations are initiated. Reviews and approves minor change controls. Created trackers on Smartsheet to track work performed by QA staff on the nightshift.
