As a Reliability Engineer, you will be the guardian of product excellence and patient safety. You will lead the reliability program for our medical devices, ensuring they perform flawlessly under real-world conditions. This is a cross-functional role where you sit at the intersection of design, manufacturing, and quality. You will be responsible for predicting product life cycles through advanced statistics and "torture-testing" hardware to identify weaknesses before they reach the market. Your work directly impacts customer satisfaction by reducing warranty claims and ensuring our life-saving technology is always ready for use.

Functie-eisen

Education: A Bachelor’s or Master’s degree in Electrical, Mechanical, Biomedical, Industrial Engineering, or Computer Science.
Experience: * With a Bachelor’s: Minimum of 2 years in reliability testing, software quality, or hardware development.
- With a Master’s: Entry-level candidates with a strong academic focus on reliability or statistics are welcome.
Technical Skills: * Proven experience with RAMS strategy and Design FMEA.
- Hands-on experience with hardware stress testing, including HALT (Highly Accelerated Life Testing) and HASS (Highly Accelerated Stress Screening).
- Proficiency in statistical analysis tools for Weibull Analysis, Monte Carlo simulations, and regression modeling.
Regulatory Knowledge: Experience working within a Quality Management System (QMS) and adhering to Good Documentation Practices (GDP) is highly preferred.
Methodology: Familiarity with Design for Reliability (DfR) and Design for Six Sigma (DfSS).

Competenties

Analytical Rigor: You have a "detective" mindset, capable of performing root cause analysis on complex failures.
Collaborative Spirit: You can work effectively with Patient Safety, Manufacturing, and Engineering teams to drive improvements.
Independence: Capable of running a reliability program with minimal oversight and taking ownership of project schedules.
Communication: Ability to provide clear technical feedback and translate complex statistical data into actionable design recommendations.
Attention to Detail: Meticulous in documenting processes to meet the high standards of medical device regulations.

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