Are you an experienced regulatory affairs professional looking for a new challenge? Our client, a leading medical device company based in Denmark is seeking a Regulatory Affairs Manager to join their team. In this role, you will be responsible for ensuring the regulatory compliance of all products within the sector.
Responsibilities:
- Generate submissions and maintain market approvals
- Ensure product compliance with relevant regulations
- Collaborate cross-functionally with other departments
- Oversee and take part in the regulatory intelligence process
Qualifications/Requirements:
- At least 10 year's experience in Regulatory Affairs within Medical Devices or In-vitro Diagnostic Devices
- Experience with cross-cultural collaboration
- Project lead experience
- Project development covering a portfolio of products
- Masters Degree in biotechnology, life sciences or engineering is preferred
With great flexibility and an impressive compensation package, this is a stand out opportunity in Regulatory affairs.
If you are interested and ready to take your next step in the world of Regulatory affairs then apply today.
