Deine Mission
QUMEA builds radar-based, contactless patient monitoring. Our RADIQ sensor platform watches over patients without cameras and without anything worn on the body, giving care teams in hospitals and long-term care reliable information on mobility, immobility and, increasingly, vital signs. We are a Swiss MedTech company with a growing presence across Switzerland, the Nordics and the wider EU, and a subsidiary in Stockholm.
New flagship use cases (respiration and immobility monitoring) and AI features are expanding our regulatory surface significantly, and we have no in-house regulatory expert embedded in product development. That is the gap you fill.
The role in one sentence
Embedded in R&D, you are the regulatory counterpart to our software, algorithm and device teams: you turn medical device requirements into concrete engineering work, own the technical documentation, and drive verification and validation.
Bewerbung
If this sounds like your dream job, we'd love to hear from you! Apply now with your CV and relevant supporting documents.