Job ad: Regulatory Affairs Specialist, Global Quality

Regulatory Affairs Specialist, Global Quality

Would you like to work with products that actually change the lives of people and do it in a worldwide, fast-growing company? And do you have experience with regulatory affairs and registration of medical devices? Then you could be the person we are looking for as our new Regulatory Affairs Specialist.

With reference to the Vice President of Global Quality, you will be part of the regulatory team responsible for the registration of products. Our team consists of three people in Middelfart and four people in Poland who are all working in the field of regulatory, quality and compliance.

Your main responsibilities will be to:

• Register medical device products - class IIa and class I worldwide
• Maintain market approvals
• Provide regulatory assistance to Customer Service and other stakeholders