Senior Manufacturing Quality Manager – Medical Devices

Confidential Recruiting Partners

  • Littleton, Massachusetts
  • 2 days ago

    Highlights

    Our client is seeking an experienced Senior Quality Manager to own manufacturing quality performance, including inspection activities, NCR/MRB processes, CAPA, and quality systems execution. 8+ years of progressive Quality experience in regulated manufacturing (medical device required; aerospace/defense/IVD acceptable with relevant crossover).

    Numbers & Facts

    LocationLittleton, Massachusetts

    Description

    Our client is seeking an experienced Senior Quality Manager to own manufacturing quality performance, including inspection activities, NCR/MRB processes, CAPA, and quality systems execution. This role is highly visible within operations and requires strong leadership, cross‑functional collaboration, and hands‑on shop‑floor engagement.

    Onsite | No Visa Sponsorship | No Relocation Assistance

    Responsibilities:

    • Audit Support: Support internal/external audits, including regulatory inspections.
    • Supplier Quality: Support incoming material quality and vendor‑related troubleshooting.
    • Quality Reporting: Provide leadership with data‑driven reporting on quality, performance and risk.
    • NCR/MRB Ownership: Lead investigation, disposition, trending, and timely closure of nonconformances.
    • CAPA & Root Cause: Drive corrective actions based on manufacturing trends and structured root‑cause analysis.
    • Manufacturing Quality Leadership: Lead all manufacturing‑related quality activities across production operations.
    • Inspection & Product Release: Oversee in‑process inspection, final inspection, product acceptance, and release.
    • Team Management: Manage Quality Engineers, the QC Supervisor, and inspection teams; coach and develop staff.
    • Continuous Improvement: Apply Lean, Six Sigma, and risk‑reduction methodologies to improve yield and efficiency.
    • Quality Systems & Compliance: Ensure compliance with ISO 13485, FDA QMSR, and other applicable regulations.
    • Cross‑Functional Collaboration: Partner with Manufacturing, Engineering, Supply Chain, and Operations to resolve issues.

    Qualifications (Must-Haves)

    • 3+ years managing Quality Engineers and/or QC teams.
    • Ability to travel 5–10% for vendor support, customer visits, and system testing.
    • Bachelor's degree in Engineering (Mechanical, Electrical, or related) or equivalent experience.
    • Strong knowledge of ISO 13485, risk‑based quality principles, and regulated QMS requirements.
    • Hands‑on ownership of manufacturing quality, including NCR/MRB, CAPA, and shop‑floor execution.
    • 8+ years of progressive Quality experience in regulated manufacturing (medical device required; aerospace/defense/IVD acceptable with relevant crossover)

    Benefits & Perks:

    • Life Insurance
    • 10% annual target bonus
    • Medical, Dental, and Vision
    • 401(k) with company match
    • Comprehensive paid leave
    • Flexible working environment

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