Job Purpose
Are you a recent science graduate curious about how health policies and EU regulations shape the medical technology field? Join MedTech Europe as a
Regulatory Affairs Intern
and gain hands-on experience at the intersection of healthcare, policy, and innovation.
You'll work closely with our In Vitro Diagnostics (IVD) and Medical Devices (MD) teams, contributing to real-world policy discussions and helping ensure that the voice of industry is heard across Europe. Expect a dynamic learning environment with exposure to high-level stakeholders, EU (health) policy processes, and international initiatives.
Responsibilities
Requirements
Nice-to-have skills
What we offer
How to apply
Please send your CV and Cover Letter, in an email with subject line "Internship application: YOUR NAME AND SURNAME" to Iana Slobodeaniuc ), Senior Manager IVD and HR at The body of the email will serve as the motivation letter and should be no longer than 250 words, answering the following questions:
Deadline for application is 15 October 2025. Suitable candidates might be contacted before this deadline, so early application is encouraged. Interview will take place on a rolling basis.
Please note that only short-listed candidates will be contacted.
The starting date is as soon as possible after approval of the CIP by the Administration.
About MedTech Europe
MedTech Europe is the European trade association for the medical technology industry including diagnostics, medical devices and digital health. Our members are national, European and multinational companies as well as a network of national medical technology associations who research, develop, manufacture, distribute and supply health-related technologies, services and solutions.