Verification and Compliance Engineer

m/f/d, Zug

Job profile (4BWC73)

Life Sciences - Quality Management
Zug
Contracting
Full Time
As soon as possible/latest start date 1.11.2026 - 6 months
Compliance, IVD, Medtech

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).

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