Senior Regulatory Affairs Specialist — MDR/FDA Global Lead

Elos Medtech AB is seeking a Senior Specialist in Regulatory Affairs located in Muntelier Yverdon-les-Bains, Switzerland. The role focuses on leading regulatory compliance activities and managing CE marking under MDR and FDA submissions.

The ideal candidate has a degree in Engineering or Life Sciences and extensive Regulatory Affairs experience in the medical device industry. The position offers an inclusive culture with opportunities for personal development, 6 weeks vacation, and attractive social benefits.