Description
The Quality System Specialist – CAPA at Merrimack Manufacturing, LLC is responsible for managing the Quality Management System (QMS) in accordance with ISO 13485 and regulatory standards for medical devices. Key duties involve coordinating, tracking, reporting, and monitoring Nonconformance (NC) and Corrective and Preventive Action (CAPA) processes, conducting root cause analyses, supporting nonconformance evaluations, assisting with change control, preparing metrics for management reviews, and providing general QMS support.
