Regulatory Affairs Consultant – Swiss MepV/IvDV
Listed on 2026-09-27
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Healthcare
Medical Science, Healthcare Compliance, Medical Device Industry, Data Scientist
Regulatory Affairs Consultant – Swiss MepV/IvDV – 7107 URA
Our client is a leading Swiss multinational healthcare company headquartered in Basel, Switzerland. Operating in Pharmaceuticals and Diagnostics, it is one of the world’s largest biotech companies and a global leader in in-vitro diagnostics and cancer treatments. Our client is known for its strong focus on innovation, particularly in personalized healthcare, and has played a major role in developing treatments for oncology, immunology, infectious diseases, and neuroscience.
The ideal candidate is a qualified German speaking professional with a degree in medical technology, natural sciences, or industrial engineering. They will have at least three years of experience in regulatory affairs or quality management within the medtech/IVD industry. Sound knowledge of the Swiss In Vitro Diagnostics Ordinance (IvDV) Swiss Medical Devices Ordinance (MepV) and practical experience in verifying third-party documentation.
This is a 6 months contract role to be working from their office in Rotkreuz in Switzerland.
- Regulatory Verification:
Independent review and evaluation of technical documentation, Declarations of Conformity (DoC), CE certificates, and markings for third-party medical devices and in-vitro diagnostics; verification of correct labeling with regard to CH-REP (Swiss Authorized Representative) and importer obligations In accordance with MepV/IvDV. - Vendor & Partner Management:
Communication with suppliers and partners to request, review, and clarify missing regulatory documentation and quality agreements. - PRRC Support:
Preparation of recommendations for the approval or blocking of third-party products for the Swiss market. - Operational support in the area of regulatory affairs as needed: e.g., supplier inquiries, document review (non-exhaustive list)
Experience:
- Relevant Swiss working/residency permit or Swiss/EU-Citizenship required
- Successfully completed degree in medical technology, natural sciences, industrial engineering, or a comparable qualification
- Regulatory expertise:
Demonstrable, several years (3+ years) of professional experience in regulatory affairs/quality management in the medtech or IVD sector - Good Knowledge of:
- Swiss Medical Devices Ordinance (MepV) and In Vitro Diagnostics Ordinance (IvDV)
- Experience with third-party processes:
Practical experience in auditing, approving, or verifying supplier and third-party documentation - Fluent German and English, both written and spoken
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