Principal Firmware Engineer

Compen Embedded

Eindhoven

On-site

EUR 70,000 - 90,000

Full time

14 days+
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Job summary

A cutting-edge medical technology firm located in Eindhoven is seeking a Principal Firmware Engineer to serve as a hands-on expert and technical consultant for medical device teams. The ideal candidate will lead the development of firmware for Class III devices, ensuring compliance with medical standards. Applicants must have a Master's/PhD in Computer Science and extensive experience in embedded development. This is an on-site role, and candidates are expected to reside in the Netherlands.

Qualifications

  • Extensive experience in embedded development, ideally in regulated environments.
  • Comfortable in a Unix CLI environment with tools like Neovim and Docker.
  • Hands-on experience with unit testing and documentation.

Responsibilities

  • Lead architecture and development of real-time firmware for Class III medical devices.
  • Act as a technical consultant to client teams on firmware design and regulatory expectations.
  • Ensure compliance with medical device standards and guide clients on best practices.

Skills

Embedded development
C++
Consulting
Firmware design
Microcontrollers
Unix CLI

Education

Master's/PhD degree in Computer Science

Tools

Neovim
Docker

Job description

Overview

Compen Embedded is an early-stage startup headquartered at the High Tech Campus in Eindhoven, providing cutting-edge technological solutions to medical device startups driving neuroscience innovation across Europe and the United States. Our mission is to help them overcome firmware challenges and fast-track the delivery of life-changing breakthroughs.

The Role

As a Principal Firmware Engineer in a consulting capacity, you'll serve as a trusted technical advisor and hands-on expert for multiple medical device teams. You'll architect firmware, guide engineering decisions, and step into complex, high-stakes environments where reliability and regulatory compliance are non-negotiable. Your work will directly influence the safety, performance, and success of next-generation medical technologies.

This is an on-site role. To be considered, applicants must currently reside in the Netherlands and hold valid work authorization.

Responsibilities
  • Lead the architecture, design, and development of real-time firmware for Class III medical devices in modern C++
  • Act as a technical consultant to multiple client teams, helping them navigate firmware design, risk management, and regulatory expectations
  • Collaborate with cross-disciplinary (external) teams including hardware, systems engineering, neuroscience, and quality assurance
  • Ensure compliance with medical device standards (ISO 13485, IEC 62304, ISO 14971) and guide clients through best practices
  • Define and implement verification and validation strategies, including unit tests, integration tests, and traceability
  • Diagnose, debug, and resolve complex firmware issues in a structured, reproducible, and client-friendly manner
  • Mentor client engineering teams, conduct code reviews, and elevate engineering practices across organizations
  • Shape internal consulting methodologies, documentation standards, and long-term technical direction at Compen Embedded
Qualifications
  • Care deeply about patient outcomes and doing things the right way, even when nobody's watching
  • Hold a Master\'s/PhD degree in Computer Science
  • Bring extensive experience in embedded development, ideally within regulated or safety-critical environments
  • Have strong consulting instincts: clear communication, expectation-setting, and the ability to build trust quickly
  • Are comfortable working across multiple projects and adapting to different engineering cultures and maturity levels
  • Have deep familiarity with microcontrollers, low-power design, real-time constraints, and hardware-software integration
  • Can read and reason about circuit diagrams across both digital and analog domains
  • Have hands-on experience with unit testing, documentation, and working in accordance with FDA/CE guidelines
  • Thrive in a Unix CLI environment, wielding tools like Neovim, tmux, and Docker with speed and precision
  • Have experience in startups (abroad), regulated environments, or connected medical devices
  • Enjoy the autonomy and ownership that come with consulting

Recruitment agencies are kindly requested not to respond to this vacancy.

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