Industry: Medical Device Area of expertise: MDR 2017/745, ISO 13485, MDSAP, FDA, Medical devices, Regulatory & Compliance, Audits, Quality Management Experience: ~4 years Country: Netherlands Sponsorship: Yes (change of the sponsor, no relocation) Roles: Regulatory Affairs Officer/Specialist , Quality Assurance Manager, Quality Management System Manager/Specialist, medical device, Medical Device, Medical Device, Medical Device, Netherlands