Test Expert

il y a 2 jours

LouvainlaNeuve, Belgique IBA Temps plein

**Requisition ID**:3401

**Location**:Louvain-la-Neuve, BE

**Work regime**:Full-Time

**Kind of contract**:Open Ended Contract

**Mission**
Join a team in our proton therapy business unit to work with our medical-grade particle accelerator technology. As a Verification Coordinator, you will be a key player in the quality assurance of mission-critical systems, ensuring every release meets the highest standards of performance and compliance. You also will be responsible for planning, coordinating, and supervising system verification activities across projects that combine software, automation and hardware components. You’ll work closely with multidisciplinary teams to ensure the system behaves exactly as expected.**Key responsibilities**
- Define verification strategies and plans including functional and performance testing, inspection, analysis
- Monitor test execution, analyze results, and document verification reports.
- Coordinate all verification activities - software, hardware, regression, and system-level testing.
- Ensure that anomalies (bugs, gaps, non-conformities) are adequately tackled in product releases.
- Continuously improve verification processes, challenge existing methods, and participate to the development of tools.
- Ensure full compliance with international medical standards (e.g. IEC / ISO / ISO 13485).

**Skills and Qualifications**

**You have**
- Master’s degree in electronics, automation, applied physics, mechanical engineering, embedded systems, or equivalent.
- 5+ years of experience in system verification, product validation or test engineering in a regulated or safety-critical environment (medical, aerospace, railway, defense...).
- Strong background in multi-level test strategies (system, integration, and unit tests, inspection, analysis ).
- Hands-on experience with requirements and test management tools (Polarion, DOORS, Helix or equivalent).
- Solid understanding of complex systems mixing software, hardware, and real-time control.
- Familiarity with medical device standards (e.g., ISO 13485, FDA Part 820).

**And you are**
- Highly organized, with a strong planning and documentation mindset.
- Assertive communicator, able to defend a verification plan in front of technical stakeholders.
- Strong transversal collaboration skills - you'll be a key link between multiple engineering teams.
- Continuous improvement mindset and attention to quality.

**What we offer**
- Permanent contract with hybrid work (Louvain-la-Neuve & remote)
- Competitive salary package (company car/cash for car, insurance, meal vouchers, etc.)
- Dynamic and innovative work environment in a global B2B tech company
- The opportunity to grow in a company that truly makes a difference in healthcare
- A high-impact, cross-functional role with real influence on product releases.
- A small, skilled team (11 people), giving you a full-system view and the ability to shape methods.

**Recruitment Process**
- **First interview** - with Luis de la Serna (Recruiter) and Thomas Vanzieleghem (Hiring Manager)
- **Second interview** - with the peers

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