Clinical & Regulatory Affairs Compliance Coordinator 80-100%
Ziemer Ophthalmic Systems AG
Port
Key information
- Publication date:19 November 2025
- Workload:80 – 100%
- Contract type:Permanent position
- Place of work:Port
Job summary
Join Ziemer Group, a leader in ophthalmology innovation. Shape the future with us!
Tasks
- Ensure regulatory compliance for medical technology products.
- Lead operational processes for clinical evaluations.
- Develop expertise in clinical & regulatory affairs.
Skills
- Experience in clinical or regulatory affairs is essential.
- Strong analytical and problem-solving skills required.
- Excellent communication and teamwork abilities needed.
Is this helpful?
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 Clinical & Regulatory Affairs Compliance Coordinator, you will play a key role in ensuring regulatory compliance and clinical evaluation of our medical technology products. You will act as the operational process owner for clinical evaluation and make a significant contribution to the further development of internal expertise in the area of clinical & regulatory affairs.
We offer you an exciting challenge in the growth-oriented medical technology market. As a committed and proactive personality, you can help shape the future of our dynamic company.
Have we aroused 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 +41 32 332 71 00. If you have any technical questions, please contact Ms. Michela Peisino, Director Regulatory Affairs, E-Mail schreiben.
Ziemer Ophthalmic Systems AG
Allmendstrasse 11
CH-2562 Port, Switzerland
