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Engineering

Senior Quality Manager – Manufacturing

Specialized Recruiting Group - Boxborough, MA

Location
Littleton, MA · On site
Compensation
$0 – $0
Job type
Direct hire
Experience
Mid-senior
Industry
Medical Devices

+$3,500 via BYOR if placed through BYOR

About the role

We are seeking an Operations Quality Manager for a manufacturing company in Littleton, MA. This role will own day-to-day manufacturing quality, lead the QC Supervisor and Quality Engineering team, and drive quality systems and continuous improvement initiatives.

Key Responsibilities

  • Lead all manufacturing-related quality activities across production operations.
  • Oversee in-process inspection, final inspection, product acceptance, and release activities.
  • Manage Quality Engineers, the QC Supervisor, and inspection activities.
  • Own the NCR/MRB process, including investigation, disposition, trending, and timely closure.
  • Drive CAPA and corrective actions based on manufacturing quality trends and root cause analysis.
  • Lead continuous improvement initiatives focused on quality, yield, efficiency, and risk reduction.
  • Apply Lean, Six Sigma, and other process improvement methodologies.
  • Support new product, equipment, and manufacturing process introductions through quality planning and risk management.
  • Ensure compliance with FDA QMSR, ISO 13485, and applicable international regulations.
  • Support internal and external audits, including FDA and notified body inspections.
  • Partner with Manufacturing, Engineering, Supply Chain, and Operations to resolve quality issues and improve processes.
  • Support supplier quality activities related to manufacturing and incoming material performance.
  • Provide leadership with data-driven reporting on quality performance, risks, trends, and improvement initiatives.
  • Coach and develop the manufacturing Quality team while helping build a strong culture of quality.

Must-haves

MUST HAVES

  • Bachelor’s degree in Engineering (Mechanical, Electrical, or related discipline) or equivalent experience and training.
  • 8+ years of progressive Quality experience in medical device, aerospace, defense, or IVD manufacturing, with some prior medical device experience required.
  • 3+ years managing Quality Engineers and/or QC teams.
  • Experience owning Manufacturing Quality, NCR/MRB processes, and shop-floor execution.
  • Strong knowledge of ISO 13485 and risk-based quality principles.
  • Must be able to travel (5-10%) to support vendors, customer sites, troubleshooting, and system testing.

Benefits

  • Competitive compensation
  • 10% annual target bonus
  • Health, vision and dental insurance
  • 401k retirement savings with match
  • Life insurance
  • Comprehensive paid leave
  • Flexible working environment

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