2 beste Stellen als regulatory affairs specialist in vaud – aktuell auf Personalsuche

Senior Specialist Regulatory Affairs
Elos Medtech —Yverdon-les-Bains, VD
- 100%
- Management-Erfahrung
- Englisch
- Kommunikationsfähigkeit
Senior Medical Scientist - Systemic Pain
Haleon —Nyon, VD
- 100%
- Erfahrung in der IT
- Kommunikationsfähigkeit
13 Tage

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Senior Medical Scientist - Systemic Pain
Haleon —Nyon, VD
The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment…
13 Tage

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Senior Specialist Regulatory Affairs

Elos Medtech -
Yverdon-les-Bains, VD

Jetzt bewerben

Details zur Stelle

100% | Pensum: 90-100%

Qualifikationen

Französisch
Management-Erfahrung
Englisch
Kommunikationsfähigkeit
Deutsch

Vollständige Stellenbeschreibung

Job Category: QA

Job Type: Full Time

Job Location: Muntelier Yverdon-les-Bains

Country: Switzerland

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&D, Quality Assurance, Clinical Affairs, and other stakeholders to support product development and market access

What makes you a great fit

Degree in Engineering, Life Sciences, or a related field, combined with several years of Regulatory Affairs experience in the medical device industry
Strong knowledge of European MDR and U.S. FDA regulations, including regulatory submissions and technical documentation
Solid understanding of clinical evaluation, biocompatibility, quality management systems, and regulatory compliance processes
Fluent in German and English, both written and spoken, French is considered an asset
Structured, proactive, and solution-oriented professional with a high level of ownership and accountability
Excellent communication and stakeholder management skills, with the ability to translate complex regulatory requirements into practical business solutions

Why you’ll love working with us

An open company culture, short decision-making processes, and an open-door philosophy
6 weeks of vacation
Attractive social benefits
Opportunities for individual development
Regular team events
Loyalty bonuses

Jetzt bewerben

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regulatory affairs specialist Jobs in vaud

Senior Specialist Regulatory Affairs

Senior Medical Scientist - Systemic Pain

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