Join our team: Regulatory Affairs Specialist

Help bring innovative diagnostic solutions to patients worldwide?

To support our expanding product portfolio and international ambitions, we are strengthening our Regulatory Affairs capabilities and are looking for an experienced Regulatory Affairs Specialist to join our Quality & Regulatory team at our headquarters in Moss, Norway.

This is an opportunity to take regulatory ownership for assigned products and projects and work across the entire IVD product lifecycle – from development and regulatory strategy to market access and post-market activities.

Learn more and apply here.