Validation Engineer II
Integra LifeSciencesAuvergne-RhĂŽne-Alpes, France
Posted April 9, 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 patientsâ 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 and contribute to creating change and shaping the future of healthcare by working as a Validation Engineer II. You will be responsible for validating processes, equipment, and software to meet regulatory requirements and internal needs.
Requirements
- Engineer degree in biomedical engineering or process engineering
- Good mastery of medical device regulation, including MDR, ISO 14971, ISO 13485, FDA, and MDSAP
- Fundamental knowledge in validation, including URS, FS, VMP, and V&V
- Ability to communicate effectively in French and English
Benefits
- Competitive salary
- Comprehensive benefits package
- Opportunities for career growth and development
