Responsable principal des affaires réglementaires 80-100%

Join Ziemer Group, a leader in ophthalmology innovation. Enjoy a dynamic work environment and growth opportunities.

Tasks

• Ensure regulatory compliance of medical devices throughout their lifecycle.
• Collaborate with R&D, Quality, Clinical, and Marketing teams.
• Share knowledge and support team development as a strong player.

Skills

• Extensive regulatory expertise with a proactive approach.
• Strong teamwork and collaboration skills.
• Ability to shape the future in medical technology.

We aim to enhance the lives of millions. Driven by our passion for innovation, we tirelessly develop cutting‑edge products and services in ophthalmology. Become a part of the Ziemer Group's 25‑year legacy and contribute to our ever‑expanding team.

As a Senior Regulatory Affairs Manager, you will play a central role in ensuring the regulatory compliance of our medical devices throughout the entire product lifecycle. You bring extensive regulatory expertise, provide professional support to the team, and work closely with interdisciplinary departments such as R&D, Quality, Clinical, Marketing, and Supply Chain. In addition to your regulatory expertise, you are a strong team player who shares knowledge, supports colleagues, and contributes to the ongoing development of the team.

We offer you an exciting challenge in a growth‑oriented medical technology market. As a dedicated and proactive individual, you will have the opportunity to actively shape the future of our dynamic company.

Have we sparked your interest? Then we look forward to receiving your complete online application.

For further information, please contact Mr. Richard Büchi, Director Human Resources, E‑Mail schreiben or . For technical questions, please reach out to Dr. Michela Peisino, Director Regulatory Affairs, E‑Mail schreiben.

Ziemer Ophthalmic Systems AG

Allmendstrasse 11

CH-2562 Port

Switzerland