NonStop Consulting
Regulatory Affairs Specialist – Medical Devices (Doesburg, the Netherlands)
Do you want your regulatory expertise to contribute to medical devices that genuinely improve patients’ lives worldwide? For a fast-growing international medical technology organization, I am looking for a Regulatory Affairs Professional with experience in medical devices.
In this role, you will manage and maintain international product registrations and ensure ongoing compliance with global regulations. You will work closely with Quality, Clinical, R&D, and Engineering teams, acting as a trusted regulatory partner. You stay on top of regulatory developments and proactively contribute to improving RA processes and ways of working.
You bring at least 3 years of experience in Regulatory Affairs within medical devices, a strong eye for detail, and the ability to manage multiple registration projects in parallel. You have an HBO level of thinking and working and communicate fluently in English.
You can expect an impactful RA role, hybrid working, strong work-life balance, plenty of room for development, and an attractive overall package.
I will be looking forward to your application
