Verification and Compliance Engineer (m/f/d) — Coopers Group AG
- Location
- Zug
- Contract
- contracting
- Posted
- 6 days ago
Role overview
In this role, you will be responsible for the independent regulatory verification and evaluation of third-party products (3rd party products) in relation to the applicable European (EU-MDR / EU- IVDR) and Swiss regulations (MedDO / IvDV).
- In this role, you will be responsible for the independent regulatory verification and evaluation of third-party products (3rd party products) in relation to the applicable European (EU-MDR / EU- IVDR) and Swiss regulations (MedDO / IvDV).
- Regulatory verification: Independent review and evaluation of technical documentation, declarations of conformity (DoC), CE certificates and markings of 3rd party medical devices and in vitro diagnostics, verification of the correct labeling with regard to CH-REP (Swiss Authorized Representative) and importer obligations according to MedDO/IvDO.
- Vendor & Partner Management: Communication with suppliers and partners to demand, review and clarify missing regulatory evidence and quality agreements.
- Life Sciences - Quality Management Contracting Full Time
- As soon as possible/latest start date 1.11.2026 - 6 months Compliance, IVD, Medtech
Main responsibilities
- Regulatory verification: Independent review and evaluation of technical documentation, declarations of conformity (DoC), CE certificates and markings of 3rd party medical devices and in vitro diagnostics, verification of the correct labeling with regard to CH-REP (Swiss Authorized Representative) and importer obligations according to MedDO/IvDO.
- Vendor & Partner Management: Communication with suppliers and partners to demand, review and clarify missing regulatory evidence and quality agreements.
- PRRC Support: Creation of recommendations for the release or blocking of third-party products for the Swiss market.
- Operational support in the area of regulatory as required: e.g. supplier enquiries, document review (non-exhaustive list) Must Haves:
- Successfully completed studies in the field of medical technology, natural sciences, industrial engineering or a comparable qualification
- Fluent in German and English, both written and spoken
- Regulatory expertise: Demonstrable, several years (3+ years) of professional experience in Regulatory Affairs / Quality Management in the medtech or IVD sector In-depth knowledge
- Focus: Swiss In-vitro Diagnostics Ordinance (IvDV) Swiss Medical Devices Ordinance (MedDO)
- Experience with 3rd party processes: Hands-on experience in auditing, approving or verifying supplier and third-party documentation Job profile Life Sciences Quality Management Zug Contracting Full Time
- As soon as possible/latest start date 1.11.2026
Key requirements
- Life Sciences - Quality Management Contracting Full Time
- As soon as possible/latest start date 1.11.2026 - 6 months Compliance, IVD, Medtech
Additional details
- Operational support in the area of regulatory as required: e.g. supplier enquiries, document review (non-exhaustive list)
- Regulatory expertise: Demonstrable, several years (3+ years) of professional experience in Regulatory Affairs / Quality Management in the medtech or IVD sector In-depth knowledge
- Focus: Swiss In-vitro Diagnostics Ordinance (IvDV) Swiss Medical Devices Ordinance (MedDO)
- Experience with 3rd party processes: Hands-on experience in auditing, approving or verifying supplier and third-party documentation Quality Management Compliance, IVD, Medtech
Notes and original content
- Responsibilities:
- Must Haves:
- Regulatory expertise: Demonstrable, several years (3+ years) of professional experience in Regulatory Affairs / Quality Management in the medtech or IVD sector
- In-depth knowledge
- Focus: Swiss In-vitro Diagnostics Ordinance (IvDV)
- Swiss Medical Devices Ordinance (MedDO)
- Experience with 3rd party processes: Hands-on experience in auditing, approving or verifying supplier and third-party documentation
- Job profile
- Life Sciences
- Quality Management
Questions about this listing
What salary does Coopers Group AG offer for this role?
Coopers Group AG lists CHF 78'500 - 119'000 gross per year for this position in Zug. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Coopers Group AG offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Coopers Group AG during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Zug?
EU/EFTA residents living in the border zone of the country adjoining Canton Zug can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Zug's cantonal migration office or with HR during the application.
How do I apply for this position at Coopers Group AG?
Use the "Apply now" button on this page — it links directly to Coopers Group AG's original listing at coopers.ch, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
