Senior Manager, Quality Assurance

KARL STORZ Endovision Inc

  • Auburn, MA
  • 30+ days ago

    Highlights

    Collaborative Leadership & Influence: You build strong cross-functional relationships, confidently lead teams through audits and quality initiatives, and communicate effectively with employees, leadership, customers, and regulatory agencies. Quality & Compliance Leadership: You have deep expertise in medical device quality systems, regulatory requirements, auditing, and CAPA processes, with the ability to drive compliance while advancing continuous improvement initiatives.

    Numbers & Facts

    LocationAuburn, MA

    Description

    About KARL STORZ

    From the operating room to surgery centers-and everywhere in between-KARL STORZ North America is a global leader in medical technology and advanced visualization solutions. We design specialty innovations, smart instruments and devices, integrated ecosystems, and intelligent imaging-to build a more connected, software-enabled operating room.

    As an independent, family-owned MedTech company, we ambitiously think in generations instead of quarters to improve patients' lives around the world.

    About the Role

    • Lead quality where it matters most-with real ownership, visibility, and influence at the site level
    • Drive meaningful impact on patient safety, customer trust, and global business performance
    • Tackle complex, high‑impact challenges across CAPA, audits, analytics, and continuous improvement
    • Partner with senior leaders and global teams-your expertise will shape decisions
    • Build and inspire a strong Quality team while advancing your own leadership career
    • If you're ready to move beyond compliance and set the standard for quality excellence, this role is built for you.

    What you'll do

    • Lead Quality Assurance, Quality Engineering, and Quality Support teams
    • Own site QMS compliance to FDA, ISO, MDR, CE, and global regulatory standards
    • Oversee CAPA, complaints, audits, management review, and quality metrics
    • Serve as Site Management Representative for audits and inspections
    • Drive continuous improvement through data analytics and quality best practices
    • Develop talent, training programs, and a strong quality culture

    What you bring

    • 10+ years of quality experience in medical devices
    • 7+ years of quality auditing experience
    • 3+ years of people leadership experience
    • Bachelor's degree; Lead Auditor certification (ISO 9001 or 13485)
    • Deep knowledge of FDA 21 CFR 820, ISO 13485, MDR, and risk management
    • Strong communication, analytics, and stakeholder‑management skills

    This role will be onsite at our office in Auburn, MA - expectation is 5 days/ week in the office.

    What Will Make You Successful

    • Quality & Compliance Leadership: You have deep expertise in medical device quality systems, regulatory requirements, auditing, and CAPA processes, with the ability to drive compliance while advancing continuous improvement initiatives.
    • Analytical & Strategic Mindset: You leverage quality, complaint, and service data to identify trends, solve complex problems, mitigate risk, and deliver actionable recommendations that improve customer outcomes and business performance.
    • Collaborative Leadership & Influence: You build strong cross-functional relationships, confidently lead teams through audits and quality initiatives, and communicate effectively with employees, leadership, customers, and regulatory agencies.

    Why KARL STORZ?

    Join KARL STORZ and be part of a team creating medical innovations that truly make a difference. Beyond technology, you'll be part of a culture that values talent as its greatest asset, empowering you to contribute to a mission that improves patient care worldwide.

    Ready to make an impact?

    Apply to be our next Senior Manager, Quality Assurance and help us build the future of MedTech together.

    #LI-NM1

    Similar Jobs