Symbios Orthopédie SA is seeking a Senior Regulatory Affairs Design Quality Engineer to enhance their Regulatory Affairs and Quality Assurance department. The successful candidate will manage regulatory interactions and ensure compliance with medical device regulations.

Applicants should have at least 7 years of experience in the medical device industry, preferably in orthopedics, with strong knowledge of EU-MDR and FDA QMSR. Fluency in French and English is required, and the role is based in French-speaking Switzerland.