Manager Regulatory Affairs for medical devices

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Manager Regulatory Affairs for medical devices

Virum

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We need a new manager for our Regulatory Affairs team. The team is responsible for laying out the regulatory strategy, implementing the approved strategy and for conducting submission/registration, clinical evaluations, and Post Market Surveillance activities for combination products.

Some of our product development projects are reaching the launch phase and we are busy supporting the global submissions and launches. You will be the manager of eight dedicated and highly skilled employees. You will work close together with two sister teams in the QA/RA organisation and other departments across the organisation as well.