Senior Regulatory Affairs Lead – Medtech (MDR/FDA)

Elos Medtech, a leader in medical technology, is seeking a Senior Specialist Regulatory Affairs for its sites in Muntelier and Yverdon-les-Bains. In this role, you'll lead the creation and maintenance of Technical Documentation and manage regulatory compliance across the product lifecycle.

The ideal candidate will hold a degree in Engineering or Life Sciences, possess regulatory experience, and be fluent in German and English. You'll enjoy a collaborative culture, 6 weeks of vacation, and attractive social benefits.