General Responsibilities
* Design, implement, and maintain firmware 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
* Some years of experience in embedded firmware development, preferably in medical or other regulated industries
* Experience in developing firmware 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
* Strong programming skills in C / C++, with experience in real-time embedded firmware development
* Familiarity with RTOS platforms (e.g., Keil FuSa RTX, FreeRTOS, Zephyr, or similar)
* Experience with low-level hardware interfaces (e.g., SPI, I2C, UART, ADC / DAC, PWM, GPIO)
* Knowledge of 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, 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
* 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
* 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
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!
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