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Regulatory Affairs Manager
1 week ago
Vitrolife Group Overview
The Vitrolife Group is a leading provider of products and services for IVF treatments globally. Our mission is to unlock the full potential of science and technology to reduce barriers towards building a family.
Our team is dedicated to delivering high-quality products and services that meet the evolving needs of our customers and patients. We are committed to innovation, quality, and regulatory compliance.
Job Summary
We are seeking an experienced Regulatory Affairs Specialist to lead our regulatory projects. The successful candidate will be responsible for providing regulatory support to new product development projects, coordinating and driving regulatory projects for existing registrations, and evaluating regulatory intelligence and its implications for new and existing products.
About You
- You have a Master's degree in Engineering, Science, or equal relevant education. You have at least a few years of technical and/or project management experience, ideally within the medical device industry or similar regulated industries.
- You are very systematic and analytical as a person, but at the same time proactive and pragmatic and able to find and seek solutions in a dynamic environment.
- You are detail-oriented, able to make decisions, and a true team player, who is proactive when it comes to forming strong relationships.
Benefits
We offer an exciting job and a salary that matches your qualifications. A committed, dynamic, and international workplace with customers and business partners worldwide. You will be part of a modern company that supports and helps each other in a positive working environment. We offer staff benefits such as a delicious canteen, fitness facilities, physiotherapist, and an active staff association.
