PSymbios 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. /ppApplicants 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. /p #J-18808-Ljbffr