Sentec

Medical Device

Verification&ValidationEngineer

$95–125k ~AI est. Therwil, Basel-Landschaft, Switzerland FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Verification & Validation Engineer at Sentec. Skills: Verification and Validation, Test planning, Test execution. Lead verification & validation planning. Coordinate verification & validation execution”

Industry & Context.

Medical Device
Problems you'll solve

Resolution of V&V findings

What They're Looking For.

Must Have

Bachelor's or Master's degree, Product and/or software testing experience, Experience in a regulated industry, Very good communication skills in English

Nice to Have

Manual and automated testing experience, Automation experience is a plus

What You'll Do.

Lead verification & validation planning

Coordinate verification & validation execution

Ensure timely delivery of evidence

Ensure end-to-end traceability

Document test evidence

Coordinate with Development

Coordinate with RA/QA

Coordinate with Systems Engineering

Coordinate with Production/Service

Clarify acceptance criteria

Drive resolution of V&V findings

Implement manual tests

Implement automated tests

Drive continuous improvements

Manage collaboration with external labs

Organize approval tests

Execute approval tests

Organize qualification tests

Execute qualification tests

Apply risk-based approach

Provide status reporting

How You'll Work.

Team & Collaboration

Cross-functional coordination; External test labs; External suppliers

Communication Scope

Technical documentation; Cross-functional coordination

Process & Methodology

V&V planning, Timeline management

Full Job Description

**Join our team as a Verification & Validation Engineer** Sentec is a Swiss-American medical device company specializing in respiratory care. Since its founding in 1999 the company utilizes a deep-tech approach that is founded on advanced science and avant-garde technologies for respiratory patients across care areas. The goal is to support enduring change in clinical practice that reduces challenges of respiratory patients, improves healthcare outcomes, and alleviates cost. Sentec applies latest scientific results and engineering technologies across the three core platforms transcutaneous monitoring, intrapulmonary percussive ventilation and electrical impedance tomography. The company researches, develops and manufactures all products exclusively in-house. **Sentec earned Kununu’s Top Company award in 2025 and 2026 ** Own and lead verification & validation (V&V) planning, coordination, and execution for development outputs at product/system level across product lines (TCM, IPV, EIT), ensuring timely delivery of objective evidence for technical documentation and approvals. **Key Responsibilities: ** * Accountable for overall V&V strategy and execution for development outputs at product/system level (verification, validation, and test evidence) * Create, maintain, and communicate the overall V&V plan (scope, methods, acceptance criteria, responsibilities, timelines) aligned with project milestones * Ensure end-to-end traceability from requirements and risk controls to test cases and results; document test evidence (protocols, reports, deviations) for incorporation into technical documentation * Coordinate closely with Development, RA/QA, Systems Engineering, and Production/Service to plan tests, clarify acceptance criteria, and drive timely resolution of V&V findings * Define test concepts and implement manual and automated tests (test cases, scripts, tools) including test method development where needed * Drive continuous improvements of the methodology to increase

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