RA Officer - international environment!

NonStop Consulting is seeking a Regulatory Affairs Officer in the Arnhem region, Netherlands. This hybrid role requires three days onsite weekly. The position involves ensuring regulatory compliance in the medical device industry, preparing registration files, and collaborating across departments. Candidates should have at least 3 years of experience in medical device registrations and strong analytical skills. The company values innovation, sustainability, and quality.
Regulatory Affairs Officer - Arnhem Region (The Netherlands) Hybrid Work | 3 Days Onsite Per Week

Are you a Regulatory Affairs professional passionate about making a real impact in the medical device industry? This is your opportunity to join a fast-growing, internationally active company that is setting the standard for innovation, sustainability, and quality in ophthalmic medical devices.

We're looking for a dedicated Regulatory Affairs Officer to join our dynamic team based in the Arnhem region. In this pivotal role, you'll ensure regulatory compliance and maintain global product registrations, helping improve the vision-and lives-of patients around the world.

Your Role As Regulatory Affairs Officer, you'll collaborate closely with colleagues across Regulatory Affairs, Quality, Clinical, R&D, and Engineering. You'll be responsible for preparing and maintaining registration files, supporting audits and submissions, and monitoring evolving legislation to ensure compliance with international standards. You'll also have the opportunity to proactively identify and implement improvements within regulatory processes.

What We're Looking For We're seeking someone who combines regulatory expertise with a sharp analytical mindset and attention to detail. You bring:

A minimum of 3 years' experience with medical device registrations

HBO working/thinking level

Proficiency in English (written and spoken)

The ability to manage multiple projects and communicate clearly across departments

Your experience and additional skills will be valued and openly discussed during the interview process.

What You Can Expect You'll join a collaborative, supportive team in a company where sustainability, innovation, and quality are at the core of everything we do. We manufacture in-house, giving us full control over production and allowing for rapid development and continuous improvement. You'll work in a culture that fosters growth and encourages initiative, while benefiting from strong regulatory expertise that ensures smooth market access worldwide.

Work Setup This is a hybrid role. While flexibility is part of our culture, presence in the office (located in the Arnhem region) is required three days per week to stay closely connected with the team and product operations.