The Role
1. Answering questions from customers
2. Supporting customer service for tenders
3. Assisting cross-functional teams with product launches
4. Reviewing promotional materials in both French and Dutch
5. Updating regulatory documents and internal databases
6. Keeping track of regulatory changes in Benelux
7. Attending internal meetings with the EU Regulatory Affairs team or project teams
8. Participating in trade associations and supporting regulatory activities for various product categories are just a few of the responsibilities that come with being a regulatory affairs specialist.
You
9. Master degree in sciences or pharmacy or equivalent
10. Previous experience in regulatory affairs of 1 year at least ideally in medical devices or in vitro diagnostics area
11. Good communication skills verbal and written in Dutch and English (French is nice to have)
12. Ability to handle several projects in parallel and interact with several functions
13. Computer skills including the office pack
Even if you don’t think you match the requirements above, still get in touch with me to discuss your career options. These requirements are a guide only with certain elements being more flexible than others and we would be happy to discuss this with you.