Verification & Compliance Specialist (m/w/d)

Posted on September 26, 2026
Randstad Multilingual Recruitment
Risch
English
Temporary
Posted on September 26, 2026

About this role

For one of our clients, a global pioneer in medical diagnostics, we are currently looking for an experienced Verification & Compliance Specialist to strengthen their Regulatory Team.


In this role, you will independently handle the regulatory verification and assessment of third-party products with regard to applicable European (EU-MDR/ EU-IVDR) and Swiss (MepV / IvDV) regulations.



General Information:
 

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  • Start date: ASAP
  • Lastest start date: 01.11.2026
  • Duration: 6 months
  • Extension: not foreseen
  • Contract type: temporary contract via Randstad (employment)
  • Work location: Rotkreuz (ZG)
  • Workload: 80-100%
  • Home Office: not possible
  • Working hours: standard




Tasks & Responsibilities:
 

  • Regulatory verification: Independent review and assessment of technical documentation, Declarations of Conformity (DoC), CE certificates, and labeling for third-party medical devices and in vitro diagnostics; verification of correct labeling regarding 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 evidence and quality agreements.
  • PRRC support: Preparation of recommendations regarding the release or blocking of third-party products for the Swiss market. Operational support in the regulatory area on an as-needed basis: e.g., supplier inquiries, document review (non-exhaustive list)


Must Haves:
 
  • Successfully completed degree in medical technology, natural sciences, industrial engineering, or a comparable qualification
  • Regulatory expertise: Proven professional experience (3+ years) in Regulatory Affairs / Quality Management within the MedTech or IVD sector
  • In-depth knowledge of Swiss In Vitro Diagnostic Medical Devices Ordinance (IvDV) and Swiss Medical Devices Ordinance (MepV)
  • Experience with third-party processes: Practical experience in auditing, approving, or verifying documentation from suppliers and third-party providers
  • Business-fluent German and English (written and spoken)
 


Sounds interesting? Apply now – we’re looking forward to receiving your applications!

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