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About the Role
This position supports the Europe, Middle East & Africa (EMEA) region in aregulatory administrative capacityday-to-day administrative tasks
While part of the Regulatory Affairs organization, this role isnot technical or strategic, but rather centered onroutine administrative supportto help ensure smooth regulatory operations across the region.
Key Responsibilities
administrative support
Maintain and update theregulatory databasewith information from internal systems and US teams
Track documentation changes and ensure accurate data entry
Communicate product certifications and updates to divisional teams
Review product change notifications for database impact
tender documentationby providing accurate regulatory materials
Assist withregulatory operationsand coordination tasks
Monitor regulation updates and support internal tracking
Suggest small improvements to existing administrative processes
Requirements
Bachelor’s degree in a relevant field (e.g., Science, Law, Communication)
Fluent in English (written and spoken)
Proficient in standard computer tools (e.g., MS Office)
Previous experience in an administrative or regulatory support role is a plus, but not required
Familiarity with medical device regulations or quality systems is an advantage
Strong attention to detail and organizational skills
Able to manage routine tasks independently and reliably
Fast learner with a conscientious and accurate work style
What We Offer
A supportive, international team environment
Flexible working hours and a non-micromanaged culture
Opportunities to interact with colleagues from diverse backgrounds
Long-term growth potential after a few years in the role
Attractive employment conditions and benefits, including:
Life insurance
Private healthcare
Sports and meal cards
Employee Assistance Program
Parental policy
Employee Stock Purchase Plan
Performance bonuses
Training and language courses
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