Verification Engineer, R&D — Medical Devices

Medela

Baar

On-site

CHF 90,000 - 130,000

Full time

14 days+

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Job summary

Medela is seeking a Verification Engineer R&D to join its team in Switzerland. You will verify electromechanical medical devices, define V&V strategies, and drive test plans and documentation to ensure safety, compliance, and performance throughout the product lifecycle.

You will coordinate cross-functional teams, lead verification activities, and contribute to IoT features while adhering to medical device standards. English fluency is essential; German is an asset.

Qualifications

  • 3–5 years in verification testing of electromechanical medical devices.
  • Experience with developing test protocols and V&V documentation.
  • Proficiency in Python; familiarity with Git and LabVIEW.
  • Knowledge of medical device standards and regulations.
  • Fluent English; German is a plus.

Responsibilities

  • Own system- and sub-system level verification aligned to architecture.
  • Define V&V strategies, plans, and reports; review tests.
  • Plan and conduct verification and testing; write protocols.
  • Perform software integration testing and system interoperability.
  • Analyze verification data and prepare regulatory documentation.
  • Lead investigations, verify deviations, validate test methods.
  • Contribute to IoT features verification.
  • Collaborate with System Architects and R&D for requirements.
  • Act as technical project leader for verification.

Skills

Verification testing
Python
Git
LabVIEW
English (C1-C2)
German (asset)

Education

Engineering degree (BSc/MSc)

Tools

LabVIEW
Git

Job description

Medela is seeking a Verification Engineer R&D to join its team in Switzerland. You will verify electromechanical medical devices, define V&V strategies, and drive test plans and documentation to ensure safety, compliance, and performance throughout the product lifecycle.

You will coordinate cross-functional teams, lead verification activities, and contribute to IoT features while adhering to medical device standards. English fluency is essential; German is an asset.

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