About the Role
Designs and develops medical-grade electronic hardware and embedded firmware, working with multidisciplinary teams to deliver safe, effective, and compliant neurostimulation devices to market.
Responsibilities
- Create and refine electronic circuitry for medical neurostimulation devices, covering schematic creation, PCB layout evaluation, and component selection
- Develop, troubleshoot, and optimize low-level firmware in C/C++ for microcontrollers within medical devices
- Plan and carry out verification and validation testing of hardware according to IEC 62304, IEC 60601-1, and relevant safety and performance standards
- Work with regulatory teams to compile and update technical documentation for CE marking under EU MDR 2017/745 and FDA 510(k) submissions
- Produce and manage design history files, risk assessments per ISO 14971, and design development plans
- Take part in formal design reviews, failure mode analyses, and investigations into product deviations
- Assist manufacturing and production teams with resolving hardware issues and enhancing production processes
- Assess and approve new components, vendors, and manufacturing methods
- Keep up to date with changes in regulatory expectations, industry standards, and best practices for medical device electronics
- Support ongoing enhancements to the ISO 13485-aligned Quality Management System
Work Arrangement
Hybrid
Team
Cross-functional
Other
- Proficiency in English required; knowledge of French or Dutch is advantageous
- 38-hour workweek schedule
- Hybrid work model available from the Liège headquarters
- Potential for career advancement as the organization's technology portfolio grows
- Immediate responsibility for key system components
