Junior Regulatory Affairs Specialist - Medicines

As our Regulatory Affairs Specialist – Medicines, you make sure that Interchemie’s veterinary medicines can legally and safely be placed on the market. In practice, this means translating scientific product information into complete and compliant regulatory dossiers that meet the requirements of different countries.

You work on registrations, renewals and variations. You prepare and maintain regulatory files, coordinate documentation with several departments, handle questions from agents and authorities, and make sure that product information, labels and packaging are aligned with what is registered. Through this work, you follow products throughout their regulatory lifecycle, from initial registration to ongoing maintenance.

You operate in a hands-on, on-site role in Waalre, with responsibility for a defined set of countries and dossiers after an initial onboarding period. The role combines regulatory content with practical follow-up, such as handling samples and supporting documentation flows that other teams depend on. Accuracy, ownership and structure are essential, as your work directly affects whether products can be marketed.

Through experience, you have learned that working in a regulated environment means following through, meeting deadlines and delivering documentation that others rely on. Ownership here is not a word on paper. It means your dossiers are complete, your files are consistent and your colleagues can depend on you.

This is not a purely administrative role. You are encouraged to think along, ask critical questions and contribute ideas on how registrations, documentation and compliance can be improved. Over time, you gain insight into the full regulatory lifecycle and gradually take on broader responsibility.