Regulatory Affairs Officers – Two Positions - Utrecht area | Hybrid working | Full-time

We are recruiting two Regulatory Affairs Officers to join an international medical device company and support a major regulatory programme covering a product portfolio marketed across 35+ countries.

The two positions sit within the same Regulatory Affairs team but have different areas of focus.

1. Regulatory Affairs Officer – Product Lifecycle

You will focus on maintaining the regulatory compliance of existing medical devices throughout their lifecycle.

Your responsibilities will include:

2. Regulatory Affairs Officer – Registration & Portfolio Management

You will focus on maintaining product registrations across international markets.

Your responsibilities will include:

What are we looking for?

You should have practical Regulatory Affairs experience within the medical device industry and be able to work relatively independently.

Depending on the position, we are particularly interested in experience with:

You do not need to cover both areas. We are looking for two complementary profiles, and your experience and interests will help determine which position is the best fit.

What can you expect?

Both positions offer long-term opportunities beyond the current regulatory programme, with exposure to wider regulatory, product and cross-functional projects.

Only candidates meeting the key requirements will be contacted.