Verification Engineer

Medela; Baar; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

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.

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

Verification testing

Python

Git

LabVIEW

English (C1-C2)

German (asset)

Ausbildung

Engineering degree (BSc/MSc)

Tools

LabVIEW

Git

Jobbeschreibung

If you are passionate about electromechanical devices and bring three to five years of experience in Verification Testing, please join our R&D team and ensure our medical devices meet the highest standards of safety and compliance. You’ll play a key role in verifying the functionality and performance and driving product quality across interdisciplinary development projects.

We are seeking a Verification Engineer R&D to join our team.

Your responsibilities

• Accountable for system and sub-system level verification, ensuring alignment with system architecture, interface specifications, and product requirements.
• Define and own Verification & Validation (V&V) strategies, including creation of V&V Plans and Reports, test case review, SOPs, and test documentation throughout the product lifecycle.
• Responsible for planning and conducting verification and testing, including engineering test protocols, verification protocols, and system acceptance testing.
• Conduct and software integration testing and verify interoperability within a system-of-systems framework.
• Analyze verification data, apply statistical methods, and prepare detailed documentation for regulatory submissions, ensuring precision, reliability, and compliance with standards.
• Coordinate and lead investigations during Verification and Validation, including anomaly resolution, damage analysis, and test method validation.
• Contribute to the verification of cloud-connected and IoT-enabled features as required by product needs.
• Collaborate cross-functionally with System Architects (SA) and R&D engineers to define core requirements, approve deviations, and support SA in system decomposition into subsystems and components for detailed analysis and effective testing.
• Act as technical project leader for verification, guiding the team, and own overall verification status.

Your skills

• Bachelor's or Master's degree in Engineering, e.g. Software, Computer Science, Biomedical, Electrical, or related fields.
• 3-5 years' experience in verification testing of electromechanical devices within medical product development.
• Experience with programming language, ideally Python. Familiar with Git and LabView.
• Solid understanding of the fundamentals of verification, of product requirements and relationship to user needs as well as (micro)-architectures, of the use cases, and of the business requirements
• Operational knowledge of medical technology, including applicable standards and cross-functional disciplines within the medical device industry.General understanding of physics principles, e.g. vacuum technology and acoustics.
• Fluent in English (C1-C2), German is an asset.

Your opportunity

At Medela, you will be joining a global community of colleagues, united by the purpose that drives our business: helping people. Medela exists to advance human health and wellbeing through knowledge-based and innovative human milk and medical vacuum solutions.

Our employees are empowered to serve this purpose in a family-owned company that is growing rapidly around the world. We value intensive exchanges, diverse perspectives, and unbureaucratic decisions. You will have the opportunity to develop at an international level, and witness the direct impact your work has on our company's success.

Due to work permit restrictions, we can only consider applications from Swiss Nationals, UK, EU citizens as well as relevant work-permit holders for Switzerland.