Medical Device Compliance Specialist
4 days ago
Vitrolife Group's Regulatory Environment
Vitrolife Group operates in a highly regulated industry, with strict guidelines and regulations governing the development, manufacture, and sale of medical devices. As a Regulatory Affairs Specialist, you will play a critical role in ensuring that our products comply with these regulations and that we maintain our ISO 13485 certification.
About You
- You have a deep understanding of regulatory requirements and standards, including ISO 13485, MDR, NMPA, and FDA regulations.
- You are proficient in identifying and mitigating regulatory risks, and you have excellent communication and collaboration skills.
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.
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