München

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!