Open opportunity
MedTech regulatory software company seeking a regulatory affairs advisor for DACH and the Nordics
About the company
This company develops an AI-powered regulatory workspace for MedTech consultancies, covering device classification, clinical evidence and regulatory change tracking, with every output linked to its source. Its minimum viable product is live, validation has been published, and initial paid pilots are under discussion.
What they are looking for
The company is looking for a regulatory affairs professional with hands-on EU MDR/IVDR experience, ideally from a consultancy background; software as a medical device (SaMD) expertise is a strong advantage. The advisor should bring a strong network among regulatory affairs consultancies in DACH and the Nordics and be comfortable leading commercial conversations to secure initial paid pilots and shape go-to-market activities. The role starts as an advisory engagement, with potential to develop into a long-term partnership with equity.
A company on Boardio at start-up stage is looking for individual advisors with expertise in DACH, Nordics and MedTech. Search: "MedTech regulatory software company seeking a regulatory affairs advisor for DACH and the Nordics". This search is currently open for applications on Boardio.
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