General Responsibilities
* Design, develop, and maintain HMI applications for embedded medical devices, ensuring a responsive, intuitive, and safe user interface.
* Implement software solutions on Embedded Linux platforms, using modern programming languages and UI frameworks.
* Collaborate closely with software architects, firmware engineers, test engineers, and technical leads to ensure feature implementation aligns with design specifications and safety requirements.
* Lead or contribute to the definition of software requirements, software architecture documentation, design reviews, code reviews, and risk assessments.
* Apply unit testing, static analysis, and best practices to ensure high software quality and maintainability.
* Support integration, debugging, and system verification activities.
* Ensure end‑to‑end traceability from requirements to implementation and testing, in line with regulatory expectations.
* Create and maintain high-quality software documentation (architecture, design, implementation, verification) to support regulatory submissions and audits.
Skills and Experience
* Bachelor’s or master’s degree in computer science, Software Engineering, Electrical Engineering, or a related field.
* Several years of professional experience in embedded HMI software development, ideally within medical devices or other regulated safety‑critical industries, with demonstrable contributions to product‑grade software.
* Strong experience in Qt-based HMI/GUI development for Embedded Linux in a product development environment.
* Demonstrated experience in software architecture and design, including design documentation and structured decision-making.
* Deep understanding of medical or safety‑critical software development processes; experience with IEC 62304 Class C is highly advantageous.
* Proficiency in C++ (modern C++ required); Python is a plus.
* Solid experience with Embedded Linux and build systems such as Yocto or Buildroot.
* Understanding of HMI design principles, usability, and user-centered development.
* Strong experience applying unit testing, static code analysis, and ensuring compliance with MISRA C++ or CERT C++ standards.
* Familiarity with communication protocols such as CAN, Ethernet, and USB.
* Working knowledge of IEC 62304, ISO 13485, ISO 14971 is an advantage.
* Experience with Git, Jira, Confluence, and Agile development practices.
* Strong problem-solving and debugging skills in complex embedded environments.
* Excellent collaboration and communication skills.
* Comfortable working in a regulated, safety-critical environment.
What we can offer you
In addition to providing you with a supportive, inclusive and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with the following:
* A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth
* Exposure to a State-of-the-Art medical device development process, in close co-operation with international clinicians
* Competitive base salary
* Variable short-term & long-term incentives
* Recognition: through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements
If you like the sound of the above and feel energized by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!