QA 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.

Working on the QA Raw Materials team.

QA