On-Site Medical Device QA Director
Job in
Lenexa, Johnson County, Kansas, 66215, USA
Listed on 2026-09-04
Listing for:
Biopharma Careers
Full Time
position Listed on 2026-09-04
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Job Description & How to Apply Below
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
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