In this role, you will assure product quality through the development of 'net-new' manual or automated test scripts. This effort should maximize the ROI while minimizing quality risks. Output consistent with department's guidelines.
In this role, you will be responsible for: completing quality inspections of finished clinical product,completing line clearance for manufacturing start-ups, and providing real-time monitoring of manufacturing processes, by conducting in-process quality inspections.
In this role, you will complete and submits all supporting customer-required documents for sample submission (including supplier submission from SQE), coordination and approval (Covisant, GQTS, Schedule A, etc).