The Associate Director, Quality Assurance, is responsible for the global strategic management and oversight of R&D Quality activities and associated staff related to Good Manufacturing Practices (GMP) for non-Energy Based Devices (EBD) and EBD Medical Devices. Activities include, but not limited to, general Product Development, Validation, and Compliance.
Monday to Friday, from 8:00 to 5:00, 3 days a week in the Raleigh office.
Quality Analyst SR • Raleigh, NC, US