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Senior Manager, Quality Assurance

KARL STORZ
Posted a month ago, valid for 14 hours
Location

Auburn, MA, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • KARL STORZ North America is seeking a Senior Manager of Quality Assurance with over 10 years of quality experience in medical devices and at least 3 years of people leadership experience.
  • The role involves leading quality teams, ensuring compliance with FDA, ISO, and other regulatory standards, and driving continuous improvement initiatives.
  • Candidates must possess a bachelor's degree and a Lead Auditor certification, along with strong analytical and communication skills.
  • This position is based onsite in Auburn, MA, with a requirement of 5 days a week in the office.
  • Salary details are not specified in the job 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

 




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