Junior medical device engineer – technical & clinical operations

About ElmediX

ElmediX is a medical technology company developing TempoCure®, an innovative medical device for controlled whole-body thermal treatment in oncology. The platform combines advanced temperature monitoring, thermal control, clinical workflow integration, and medical-device engineering.

To support the clinical deployment of the TempoCure Platform during our clinical trials, we are looking for a motivated junior engineer with a strong technical mindset, practical skills, and the ambition to grow in medical device development and clinical operations.

Role

As Junior Medical Device Engineer – Technical & Clinical Operations, you will support testing, production transfer, and clinical use of the TempoCure Platform.

This is an entry-level/junior position for an engineer who is comfortable working in both a technical development environment and a clinical setting. The role combines engineering work, device testing, support of production activities, technical troubleshooting, and clinical trial support as a sponsor representative.

Key Responsibilities:

1. Device Development, Testing & Optimization

• Perform hands-on assembly and testing of device components, subsystems, and system-level performance in a controlled environment.
• Support troubleshooting, root-cause analysis, and implementation of technical improvements.
• Assist in verification and validation activities, including preparation and execution of test protocols.
• Work in accordance with ElmediX’s procedures and quality requirements.
• Maintain accurate records of performed work, tests, and production activities.

2.Clinical Trial Technical Support

• Support the technical operation of the TempoCure Platform at clinical sites.
• Train and support local clinical site teams in the correct preparation and use of the device.
• Assist in device setup, operational checks, treatment support, troubleshooting, and post-use follow-up.
• Ensure that clinical use of the device is conducted in accordance with applicable procedures and study requirements.
• Travel to clinical sites within Europe as required, including occasional multi-day site visits.

Required Profile

• Master’s degree in engineering, including Industrial Engineering, Civil Engineering, Medical Engineering, Electrical Engineering, Mechanical Engineering, or a closely related discipline.
• Entry-level or junior profile, typically 0–3 years of professional experience.
• Strong practical/manual skills and willingness to perform hands-on technical work in a controlled production or laboratory environment.
• Good understanding of metrology, measurement systems, testing, and technical problem-solving.
• Structured working style with attention to detail, safety, traceability, and procedural compliance.
• Communicative, organized, calm, and reliable in clinical or time-sensitive situations.
• Willingness to travel regularly within Europe to support clinical trial activities.
• Fluent written and spoken English.

Nice to Have

The following are considered assets but are not required. We are open to training the right junior candidate.

• Basic knowledge of ISO 13485, MDR, ISO 14971, or related medical-device standards.
• Experience or academic exposure to medical-device development, testing, production, verification, or clinical support.
• Experience with sensors, temperature measurement, electronics, data acquisition, or control systems.
• Programming or data-analysis skills, for example in Python, MATLAB, LabVIEW, or similar tools.
• Knowledge of Dutch, French, or Spanish.

What We Offer

• A full-time position in a growing medical technology company.
• A varied role at the interface of engineering, production, clinical research, and medical-device development.
• The opportunity to work on an innovative medical device platform with direct clinical application.
• Workplace in the Leuven–Mechelen area, with travel within Europe as required.
• A competitive salary and benefits package.

Application

Interested candidates are invited to submit their CV and a short motivation letter explaining their technical background, hands-on experience, and interest in medical-device development and clinical applications.