General Responsibilities

• Mentor a team of embedded software engineers, fostering technical growth and guiding day-to-day activities.
• Design, implement, and maintain software for microcontroller-based medical devices, ensuring compliance with safety and regulatory standards.
• Work with RTOS-based systems, focusing on real-time performance, reliability, and efficient resource usage.
• Collaborate with architects, test engineers, and system engineers to define interfaces, hardware abstraction layers, and low-level drivers.
• Participate in code reviews, design reviews, and risk assessments to ensure high code quality and adherence to design constraints.
• Apply unit testing, static code analysis, and other industry best practices for safety-critical software.
• Support integration testing, debugging, and root cause analysis of issues arising in system-level testing (e.g., HIL/SIL).
• Develop and maintain technical documentation, including software design, implementation details, and traceability to requirements.
• Contribute to continuous improvement of development processes, toolchains, and testing frameworks.

Skills and Experience

• Bachelor’s or Master’s degree in Electronics, Computer Engineering, Embedded Systems, or a related field.
• Several years of experience in embedded software development, preferably in medical or other regulated industries.
• Experience in developing software for microcontrollers (e.g., STM32, NXP, Renesas) in a real-time environment.
• Knowledge of regulatory and quality requirements for medical device development is an advantage.
• Expert level programming in C/C++ for real-time embedded systems.
• Deep knowledge of RTOS platforms (e.g., Keil FuSa RTX, FreeRTOS, or similar).
• Extensive experience with microcontrollers and low-level hardware interfaces (e.g., SPI, I2C, UART, ADC/DAC, PWM, GPIO).
• Experience in software development for safety-critical systems, preferably in compliance with IEC 62304, ISO 13485, and ISO 14971.
• Experience with unit testing, static analysis tools (e.g., Polyspace, Vectorcast, Axivion, Cppcheck, PC-lint, Coverity), and code coverage analysis.
• Familiarity with version control (e.g., Git), issue tracking, and CI/CD pipelines for embedded projects.
• Understanding of CAN protocols, digital I/O, and embedded debugging tools (e.g., oscilloscopes, logic analyzers, JTAG/SWD).
• Basic knowledge of hardware schematics and datasheets is a plus.
• Experience with Vector tools (vTestStudio, CANoe) is a plus.
• Strong problem-solving and analytical skills.
• Good communication skills and ability to work in cross-functional teams.
• Proactive, detail-oriented, and committed to producing high-quality and maintainable code.
• Demonstrated experience in leading teams or mentoring junior engineers.
• Comfortable working in a regulated environment with structured development processes.
• Occasional travel may be required

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