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Quality Operations Manager

Job in Littleton, Middlesex County, Massachusetts, 01460, USA
Listing for: SnapX.ai
Full Time position
Listed on 2026-08-22
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Engineering, Production QC/QA
Salary/Wage Range or Industry Benchmark: 110000 - 150000 USD Yearly USD 110000.00 150000.00 YEAR
Job Description & How to Apply Below

Company Description SnapX.ai is a next-generation freelance recruiting portal that combines AI agents with human expertise to deliver highly qualified talent for diverse hiring needs. Organizations can post a job and quickly receive applicants sourced through a network of 1,000+ freelance recruiters. The platform is designed to streamline recruitment workflows, improve candidate quality, and reduce time-to-hire. SnapX.ai focuses on creating efficient, technology-enabled hiring experiences for both clients and talent professionals.

Operations

Quality Manager - Manufacturing | Littleton, MA

We are seeking an experienced Operations Quality Manager to lead day-to-day manufacturing quality, oversee inspection activities, and drive continuous improvement initiatives. This is a high-visibility leadership role managing the QC Supervisor and Quality Engineering team, ensuring compliance with FDA and ISO standards while building a strong culture of quality.

Responsibilities
  • Lead all manufacturing quality activities across production operations.
  • Oversee in-process inspection, final inspection, product acceptance, and release.
  • Manage Quality Engineers, QC Supervisor, and inspection teams.
  • Own the NCR/MRB process including investigation, disposition, trending, and closure.
  • Drive CAPA and corrective actions based on root cause analysis.
  • Lead continuous improvement initiatives focused on yield, efficiency, and risk reduction.
  • Apply Lean, Six Sigma, and process improvement methodologies.
  • Support new product, equipment, and process introductions through quality planning.
  • Ensure compliance with FDA QMSR, ISO 13485, and international regulations.
  • Support internal/external audits including FDA and notified body inspections.
  • Partner cross-functionally with Manufacturing, Engineering, Supply Chain, and Operations.
  • Provide leadership with data-driven reporting on quality performance and risks.
  • Coach and develop the manufacturing Quality team.
Requirements
  • Bachelor's degree in Engineering, Quality, Manufacturing, or related field.
  • 7+ years of manufacturing quality experience.
  • 3+ years in supervisory or leadership roles.
  • Strong knowledge of quality tools (SPC, FMEA, CAPA, root cause analysis).
  • Experience with ISO 13485, FDA QMSR, and regulated manufacturing environments.
  • Lean/Six Sigma experience preferred.
  • Excellent analytical, organizational, and leadership skills.
Benefits
  • Competitive compensation package.
  • Annual performance bonus.
  • Health, vision, and dental insurance.
  • 401k retirement savings with match.
  • Life insurance and comprehensive paid leave.
  • Flexible working environment.
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