Associate Director, Device Quality Assurance - Hybrid

Merck Sharp & Dohme Corp

Wilson, North Carolina, United States
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
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5 years qa experience in medical devices
Device assembly and packaging operations knowledge
Iq/oq/pq and ppq validation activities
** Merck Sharp & Dohme Corp is seeking an Associate Director for Device Quality Assurance to oversee quality support in device assembly and packaging operations at their Wilson, NC site. The role requires significant experience in medical device quality assurance and offers a hybrid work model with competitive salary and benefits. **

Job Summary

  • This role serves as the primary interface between Research & Development DQ&R and the Wilson, NC site for device quality oversight.
  • The successful candidate will be accountable for coordinating triage, root cause investigations, and CAPA processes for device assembly operations.
  • Employees are eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k).

Matching Summary

Match Score: 75

** Merck Sharp & Dohme Corp is seeking an Associate Director for Device Quality Assurance to oversee quality support in device assembly and packaging operations at their Wilson, NC site. The role requires significant experience in medical device quality assurance and offers a hybrid work model with competitive salary and benefits. **

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive available; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • 5 years QA experience in medical devices
  • Device assembly and packaging operations knowledge
  • IQ/OQ/PQ and PPQ validation activities
  • CAPA management and root cause investigation
  • Design control and verification familiarity

Nice-to-have

  • Strong cross-functional partnership skills
  • Culture of early issue surfacing
  • Experience with global matrix organization
  • Innovative problem-solving abilities

Key Requirements

  • Bachelor's degree in relevant discipline
  • 5 years relevant QA experience in medical device manufacturing
  • US residency required (no visa sponsorship)

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter