Regulatory Affairs Expert with Global Impact

1 week ago


Århus, Århus Kommune, Denmark Vitrolife Group Full time
About Vitrolife Group

We unlock the full potential of science and technology to reduce barriers towards building a family.

Job Overview

A Regulatory Affairs Specialist is required to lead our regulatory projects, driving continued sales growth globally.

Key Responsibilities
  • Provide regulatory support to new product development projects.
  • Coordinate and drive regulatory projects for existing registrations.
  • Translate regulatory requirements into product design specifications.
  • Evaluate regulatory intelligence.
  • Review change controls.
About You
  • You are a curious and passionate RA Specialist with both regulatory knowledge and general technical interest in hardware and software.
  • You hold a Master's degree in Engineering, Science, or equivalent relevant education, and have at least a few years of technical and/or project management experience, preferably within the medical device industry or similar regulated industries.
  • You are systematic and analytical, proactive and pragmatic, detail-oriented, able to make decisions, and a true team-player who is proactive when it comes to forming strong relationships.
  • You are fluent in English. Preferably you are also fluent in Danish.
Our Offer

An exciting job, a salary that matches your qualifications, and a dynamic international workplace with customers and business partners worldwide.

A committed and positive working environment, where you can look forward to staff benefits such as a delicious canteen, fitness facilities, physiotherapist, and an active staff association.

Become Part of Our Mission

Vitrolife Group supports and helps each other in a positive working environment. We are passionate about our work and proud to be the market leader in a niche where we help childless people fulfill their dream of having children.



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