Global Registrations Specialist

Are you detail-oriented, organized, and eager to contribute to the rapidly growing world of medical devices and in-vitro diagnostics (IVDs)? Join our Global Registrations Team and play a key role in helping companies bring life-changing medical products to market!

What You’ll Do

As a Global Registrations Specialist, you will be the go-to expert supporting our clients in registering their Medical Device and IVD products, ensuring smooth market access. Your primary focus will be the UK market, where you’ll:

• Collect, structure, and assess regulatory documentation for product registrations;

• Submit registration files to the relevant UK health authorities and maintain up-to-date planning;

• Serve as a key point of contact for clients, providing expert regulatory guidance;

• Collaborate with internal teams, external partners, and regulatory bodies to ensure compliance;

• Stay informed about evolving regulatory requirements to support clients effectively.

You’ll work in an international, fast-paced environment and report to the Team Manager Global Registrations.

What You Bring to the Team

• Strong administrative background with an MBO+ working and thinking level;

• Experience in handling documentation & maintaining structured records;

• Affinity with the MedTech industry (a plus!);

• Excellent communication skills (written & verbal) to support a diverse range of clients, from startups to multinational corporations;

• A service-oriented mindset, with strong attention to detail and organization;

• Ability to work independently while thriving in a collaborative, international setting;

• Fluent in English (Dutch is a plus);

• Available at least 20 hours per week, with at least one office day per week in Arnhem.