Regulatory Affairs Officer – MDR & Technical Documentation
Utrecht area | €50,000–€65,000 gross/year | Hybrid working
We are recruiting a Regulatory Affairs Officer to join an established Regulatory Affairs team within an international medical device company based in the Utrecht area.
The role
You will help maintain regulatory compliance throughout the product lifecycle, including:
Your profile
Experience limited to international registrations, clinical documentation or pharmaceutical Regulatory Affairs does not meet the requirements of this role.
Package
Interested?
Please send your English CV to t.perriaux@eurolondon.com for a confidential discussion, highlighting your experience with EU MDR Technical Documentation / Technical Files.
Only candidates meeting the key requirements will be contacted.
Check our offers on www.eurolondon.fr.

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