Quality Compliance Manager - ECMP Site Facilitator
Integra LifeSciencesNeuchâtel, Switzerland • Baden-Württemberg, Germany • Ireland • Auvergne-Rhône-Alpes, France
Posted January 6, 2026
Full Time
About the Company
Integra LifeSciences is a world leader in medical technology with headquarters in Princeton, New Jersey. We are driven by our purpose of restoring patients’ lives. We innovate treatment pathways to advance patient outcomes and set new standards of surgical, neurologic, and regenerative care. We offer a comprehensive portfolio of high quality, leadership medical technology brands. Our company has offices, manufacturing and research facilities in Asia, Australia, Europe, Middle East, and the Americas. For the latest news and information about Integra and our products, please visit www.integralife.com.
Job Description
Join Integra LifeSciences to provide tactical support and oversight of the implementation of the Enterprise Compliance Master Plan at sites, developing individual site project plans and ensuring their execution according to the defined timeline and plan.
Requirements
- Bachelor's degree in Engineering, Science, or closely related technical discipline
- 10+ years of experience leading a team or equivalent education and years of management experience
- Professional level of English, French, and German knowledge verbal and written
- Experience working Quality Management Systems and understanding compliance
- Experience in highly regulated industries, medical device, and/or pharmaceutical, including material remediation experience
- Demonstrated management and communication skills
- Strong attention to detail skills
- Strong communication and presentation skills
