Quality Manager - Medical Manufacturing
Listed on 2026-07-14
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Quality Assurance Manager - Medical Manufacturing
Location: Hillsborough County, New Hampshire, United States (On-site)
Employment Type: Full-Time, Exempt, Direct Hire
Estimated Salary: $125,000 - $135,000+ per year (DOE)
Elite Leadership Talent Wanted:
Direct Hire via Medix
Medix’s specialized Life Sciences division has been retained by a world-class medical device manufacturing organization experiencing unmatched expansion. We are seeking a hands‑on, strategic Quality Manager for a Direct Hire placement at their facility in Hillsborough County. Our client invests heavily in their people, technology, and facilities, making this an incredible environment for an empowered leader to turn great ideas into action.
The Opportunity: In this role, you will provide leadership for the site Quality Assurance team and partner closely with Manufacturing, Engineering, and executive leadership to drive a culture of continuous improvement and operational excellence.
- Team Leadership: Lead, coach, develop, and mentor the Quality Assurance team while fostering accountability.
- QMS Management: Maintain and continuously improve the Quality Management System (QMS), ensuring strict compliance with FDA, ISO, and customer requirements.
- Continuous Improvement: Lead cross-functional root cause investigations and corrective actions (CAPA) for internal, supplier, and customer issues.
- Operational Performance: Monitor key metrics including scrap, rework, cost of quality, and RMAs to drive targeted improvement initiatives.
- NPI Support: Lead capability studies, PFMEA/FMEA activities, and quality planning for new and existing products.
What We’re Looking For:
- Bachelor’s degree in Engineering, Quality, Manufacturing, or a related technical field (or equivalent experience).
- 5+ years of progressive quality experience in a manufacturing environment.
- Previous supervisory or leadership experience managing quality professionals.
- Expert knowledge of QMS systems, CAPA, root cause tools, and FMEA activities.
- Strongly Preferred: Experience in medical device manufacturing or highly regulated manufacturing environments.
Please note:
Sponsorship and relocation are not available for this position.
Want to step into an empowered leadership role where your impact is visible? Apply today!
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