Senior Specialist Regulatory Affairs

Elos Medtech is one of the world’s leading development and manufacturing partners for companies in the medical technology sector. With sites in Switzerland, Sweden, Denmark, Germany, China, and the United States, we specialize in the production of implants, instruments, and components for medical technologies. We are looking for individuals who share our values — passion, trust, and results — so we can grow together and achieve even greater success. If you are ready to give your best and join an environment that values collaboration and commitment, we look forward to receiving your application. For our site in Muntelier and/or Yverdon-les-Bains, we are looking for a Senior Specialist Regulatory Affairs (a) What we are looking for Lead the creation and maintenance of Technical Documentation throughout the product development lifecycle Own regulatory strategy and compliance activities across the entire product lifecycle Manage CE marking activities under MDR and FDA regulatory submissions Ensure regulatory compliance and product registrations in international markets Lead Post-Market Surveillance (PMS), vigilance, and market monitoring activities Act as the primary liaison with notified bodies, regulatory authorities, and external partners Monitor evolving regulatory requirements and drive their implementation within the Quality Management System Partner closely with R