Sr Manager, Quality and Regulatory Operations

Posted 2 Days Ago
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Neuchâtel, CHE
In-Office
Senior level
Healthtech
The Role
Leads regulatory and quality operations for medical devices, supporting compliance, market access, tenders, and commercial success. Oversees EUDAMED, UDI frameworks, regulatory records, QMS processes, CAPA, change control, deviations, audit readiness, and compliant documentation. Partners with commercial, contracts, and cross-functional teams to interpret requirements, identify gaps, and implement solutions. Requires extensive EU medical device regulatory and quality experience, including EU MDR, CE marking, ISO 13485, and people or matrix leadership.
Summary Generated by Built In

 

Bring more to life.

 

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?


At Masimo, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. 


You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.


Masimo is a global medical technology company that develops and produces a wide array of industry-leading monitoring technologies, including non-invasive measurements, sensors, patient monitors, and automation and connectivity solutions. Our mission is, Masimo innovations empower clinicians to transform patient care. When you join our team, you’ll be part of a culture that’s driven by passion, challenging the status quo, and making an impact in the lives of others.

 

Learn about the Danaher Business System which makes everything possible.


The Sr Manager, Quality and Regulatory Operations will lead regulatory and quality operations to support compliance, market access, and commercial success. This role combines regulatory expertise with quality systems leadership to ensure products, processes, and documentation meet EU and global requirements.


The individual will act as a key partner to Commercial, Contracts, and cross-functional teams to support tender readiness, interpret regulatory and quality requirements, identify gaps, and implement practical solutions. This role requires strong expertise in medical device regulatory frameworks, quality systems, labeling, and post-market compliance, along with the ability to drive operational excellence and audit readiness

 

This position reports to the Sr Director, Quality & Regulatory Strategy and is part of the Quality Compliance team located in Neuchâtel, Switzerland and will be an on-site role.  


In this role, you will have the opportunity to:

  • Lead RA/QA operations strategy and execution to support compliance and business growth
  • Drive regulatory and quality support for tenders, including requirement review, gap assessment, and compliant documentation
  • Oversee EUDAMED compliance (actor registration, device data, vigilance) and support maintenance of regulatory records
  • Support implementation and maintenance of UDI frameworks, ensuring alignment with EU and global UDI requirements
  • Manage and improve Quality Management System (QMS) processes, including CAPA, change control, deviations, and audit readiness

 

The essential requirements of the job include:

  • 8–12+ years of experience in Regulatory Affairs and/or Quality Assurance within the medical device industry
  • Strong knowledge of EU MDR (2017/745), CE marking requirements, and European regulatory frameworks
  • Hands-on experience with EUDAMED and UDI implementation in alignment with global frameworks
  • Strong experience in Quality Management Systems (ISO 13485), including CAPA, audits, change control, and compliance processes
  • Fluent in English, any other language is a plus.

 

It would be a plus if you also possess previous experience in:

  • Patient monitoring, hospital-based medical devices, digital health, or software-enabled medical technologies
  • 3–5+ years of people leadership or matrix leadership experience, including mentoring and influencing cross-functional teams
  • Working in EU-focused or global medtech organizations with exposure to multi-country quality and regulatory operations

 

Masimo, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Skills Required

  • 8–12+ years of experience in Regulatory Affairs and/or Quality Assurance within the medical device industry
  • Strong knowledge of EU MDR (2017/745), CE marking requirements, and European regulatory frameworks
  • Hands-on experience with EUDAMED and UDI implementation aligned with global frameworks
  • Strong experience with Quality Management Systems, including ISO 13485, CAPA, audits, change control, and compliance processes
  • Fluent in English
  • Experience with patient monitoring, hospital-based medical devices, digital health, or software-enabled medical technologies
  • 3–5+ years of people leadership or matrix leadership experience, including mentoring and influencing cross-functional teams
  • Experience working in EU-focused or global medtech organizations with multi-country quality and regulatory operations exposure

Danaher Corporation Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Danaher Corporation and has not been reviewed or approved by Danaher Corporation.

  • Healthcare Strength — Healthcare coverage is described as comprehensive, including medical plan options alongside dental, vision, life, disability, and mental health support. Wellness initiatives and support programs such as an EAP and vaccination or fitness offerings add breadth beyond core insurance.
  • Retirement Support — Retirement benefits include a 401(k) plan with employer matching and options such as pre-tax and Roth contributions. Broader financial rewards such as performance bonuses and access to equity or an employee stock purchase plan are also described.
  • Parental & Family Support — Parental leave and family-building support are described as available, including maternity and paternity leave and fertility assistance. Childcare and eldercare support are also highlighted as part of the overall package.

Danaher Corporation Insights

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The Company
HQ: Washington, DC
57,802 Employees
Year Founded: 1984

What We Do

Danaher is a global science and technology innovator committed to helping our customers solve complex challenges and improve quality of life around the world. A global network of more than 25 operating companies, we drive meaningful innovation in some of today’s most dynamic industries through our operating companies in four strategic platforms: Life Sciences, Diagnostics, Water Quality and Product Identification. The engine at the heart of our success is the Danaher Business System (DBS), a set of tools that enables continuous improvement around lean, growth and leadership. Through the ingenuity of our people, the power of DBS and the impact of our meaningful technologies, we help realize life’s potential in ourselves and for those we serve.

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