Senior Firmware Engineering (m/f/d)

Join to apply for the Senior Firmware Engineering (m/f/d) role at LivaNova 3 days ago Be among the first 25 applicants Join us today and make a difference in people\’s lives! Position Summary We are looking for an experienced and results-oriented Senior Firmware Engineer with proven leadership capabilities to join our team developing software for Heart‑Lung Machines and other safety‑critical medical devices. In this role, you will design, implement, and test low‑level embedded software for microcontroller‑based systems. You will collaborate with cross‑functional teams to ensure IEC 62304 Class C compliance. Reporting to the Firmware Engineering Manager, you will contribute to the delivery of robust and reliable embedded software for life‑saving technologies. 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 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! Valuing Different Backgrounds LivaNova values equality and diversity. We are committed to ensuring that our recruitment process is fair, transparent and free from unlawful discrimination. Our selection process is driven by the key demands/requirements for the role rather than bias or discrimination on the basis of a candidate’s sex, gender identity, age, marital status, veteran status, non‑job‑related disability/handicap or medical condition, family status, sexual orientation, religion, color, ethnicity, race or any other legally protected classification. Notice To Third Party Agencies Please note that we do not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Recruitment Services Agreement, we will not consider, or agree to, payment of any referral compensation or recruiter fee. In the event that a recruiter or agency submits a resume or candidate without a previously signed agreement, we explicitly reserve the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency. Beware Of Job Scams Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons posing as LivaNova recruiters or employees. The scammers may attempt to solicit confidential, personal information, such as a social security number, or your financial information. LivaNova will never ask for fees prior/during/after the application process, nor will we ask for banking details or personal financial information in return for the assurance of employment. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for \“See Open Jobs\“ on Website, and check that all recruitment emails come from an @livanova.com email address. Job Details Seniority level: Mid‑Senior level Employment type: Full‑time Job function: Engineering and Information Technology Industries: Medical Equipment Manufacturing #J-18808-Ljbffr