Position requirements

• Bachelor’s /master’s degree in science, engineering, or equivalent degree/experience in a relevant discipline.
• Minimum 5 years Quality (QA/QS/QC/Compliance) experience with medical devices manufacturing and/or medical devices quality systems.
• Thorough understanding of ISO 13485 & ISO 14971.
• Excellent interpersonal, collaborative, and organizational skills.
• Ability to communicate effectively in French and English (German is a plus).

We offer a very dynamic work environment within a small and highly motivated team. Our customer base is very diverse and provides great exposure to very varied technical challenges and use cases.