Associate Director, Device Quality Assurance - Hybrid

med-in.at

Wilson, North Carolina, United States
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid (3 days on-site, 1 day remote)
5 years medical device qa experience
Device assembly and packaging operations knowledge
Design verification and design control familiarity
The Associate Director of Device Quality Assurance at med-in.at in Wilson, North Carolina, is a hybrid role focused on overseeing quality support for medical device assembly and packaging operations. The position requires significant experience in quality assurance within the medical device industry and emphasizes collaboration across functions to ensure product quality and patient safety

Job Summary

  • This role serves as the primary interface between Research & Development and the Wilson, NC site for device quality oversight.
  • The successful candidate will be accountable for coordinating triage, root cause investigations, and CAPA activities 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: 85

The Associate Director of Device Quality Assurance at med-in.at in Wilson, North Carolina, is a hybrid role focused on overseeing quality support for medical device assembly and packaging operations. The position requires significant experience in quality assurance within the medical device industry and emphasizes collaboration across functions to ensure product quality and patient safety.

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 medical device QA experience
  • Device assembly and packaging operations knowledge
  • Design verification and design control familiarity
  • IQ/OQ/PQ and PPQ validation expertise
  • CAPA coordination and effectiveness checks

Nice-to-have

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

Key Requirements

  • Bachelor's degree in relevant discipline
  • 5 years relevant experience in medical device QA
  • US or Puerto Rico residency required

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

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