Regulatory Affairs Expert with Global Impact
1 week ago
We unlock the full potential of science and technology to reduce barriers towards building a family.
Job OverviewA 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.
- 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.
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 MissionVitrolife 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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