On-Site Medical Device QA Director

Merck is seeking an Associate Director, Device Quality Assurance to provide quality oversight of our Device Quality & Regulatory network. The role is based on-site at the Wilson, NC site and serves as the primary interface between R&D DQ&R and the Wilson site, ensuring device assembly and packaging operations meet quality and regulatory standards.

Responsibilities include leading on-site QA for transfer activities, IQ/OQ/PQ and PPQ, CAPA coordination, risk assessments input, cross-functional