RA Officer – Work on innovative products

Location:

Arnhem – Gelderland, Nederland, Netherlands

Salary:

Negotiable

Type:

Permanent

Main Industry:

Search Health, Nursing & Social Services Jobs

Advertiser:

NonStop Consulting

Job ID:

131926564

Posted On: 

19 May 2025

Regulatory Affairs Officer – Arnhem Region, The Netherlands
Hybrid | 3 Days Onsite per Week

Are you a Regulatory Affairs professional eager to make a meaningful difference in the medical device industry? This is your chance to join a fast-growing, international company that’s redefining innovation, quality, and sustainability in ophthalmic medical devices.

We’re looking for a dedicated Regulatory Affairs Officer to strengthen our team in the Arnhem region. In this key role, you’ll help ensure global regulatory compliance and maintain product registrations that ultimately improve patients’ vision-and lives-worldwide.

Your Role

As Regulatory Affairs Officer, you’ll work cross-functionally with teams in Regulatory Affairs, Quality, Clinical Affairs, R&D, and Engineering. Your responsibilities will include:

Preparing and maintaining international registration files
*

Supporting audits, submissions, and external inspections
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Monitoring regulatory changes and ensuring compliance with evolving standards
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Proactively identifying and implementing process improvements

What We’re Looking For

We’re seeking someone who combines solid regulatory expertise with a proactive, detail-oriented mindset. Ideally, you bring:

3+ years of experience with medical device registrations
*

HBO-level education or equivalent experience
*

Excellent command of English, both written and spoken
*

Strong project management and cross-functional communication skills

Additional experience or skills? Let’s talk about them during the interview-your full profile matters to us.

What You Can Expect

You’ll be part of a collaborative and supportive environment where innovation and sustainability are central to our mission. With in-house manufacturing, we maintain full control over our products, enabling rapid development and high-quality standards. You’ll gain hands-on exposure to the entire product lifecycle and contribute to solutions that make a real-world impact.

Work Setup

This is a hybrid position, requiring 3 days per week onsite at our facility in the Arnhem region. We value flexibility-but also believe in staying closely connected with our teams and operations.

Interested? Let’s connect.
Your next step in Regulatory Affairs could start here.

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