Associate Director, Device QA & Regulatory (On-site)

Merck & Co., Inc. in Wilson, NC is seeking an Associate Director of Device Quality Assurance to provide on-site quality oversight for medical device and combination product operations.

The role interfaces with R&D DQ&R and coordinates CAPA, changes, and audit support at the Wilson site. The candidate will bring 5+ years of QA experience in medical devices, strong communication and cross-functional collaboration skills, and a track record of driving quality improvements in a matrix organization.