Associate Director, Quality Assurance

Merck • Richmond, VA, United States • Posted June 29, 2026

Location Richmond, VA
Job Type Full-time
Category other-general
Posted June 29, 2026
**Job Description**

**Position Overview - Basic Functions & Responsibility Essential function(s) includes, but is not limited to:**

Reporting to the Senior Director of Device Quality and Regulatory (DQ&R), the Associate Director Quality Engineering & Quality Assurance is responsible for independent compliance support of Medical Devices including the device constituent part of Combination Products. This position will interact with cross functional teams working with all levels of employees. Activities will include developing, documenting, and maintenance of technical business solutions, reviewing and approving medical device/combination product documentation to support regulatory filings and audits of data, policies, procedures, and systems to ensure compliance with Medical Device (21CFR 820s) and Combination Product current Good Manufacturing ruling (21CFR part 4), Device Risk Management (ISO 14971) and other worldwide regulations and company requirements. This positi...

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