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Firmware engineer (m/f/d)

Ne
LivaNova
Pubblicato il 26 novembre
Descrizione

Ph3Firmware Engineer (m/f/d) /h3 pAs a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, bwe don’t just treat conditions — we aspire to alter the course of lives. /b /p h3Position Summary /h3 pWe are looking for a passionate and skilled bEmbedded Firmware Engineer /b to join our team developing software for bHeart‑Lung Machines and other safety‑critical medical devices /b. In this role, you will design, implement, and test low‑level embedded firmware for bmicrocontroller‑based systems /b, working closely with hardware and software teams to ensure bIEC 62304 Class C /b compliance. Reporting to the bLead, Embedded Firmware Engineering /b, you will contribute to the delivery of robust and reliable firmware for life‑saving technologies. /p h3General Responsibilities /h3 ul liDesign, implement, and maintain firmware for microcontroller‑based medical devices, ensuring compliance with safety and regulatory standards /li liWork with RTOS‑based systems, focusing on real‑time performance, reliability, and efficient resource usage /li liCollaborate with architects, test engineers, and system engineers to define interfaces, hardware abstraction layers, and low‑level drivers /li liParticipate in code reviews, design reviews, and risk assessments to ensure high code quality and adherence to design constraints /li liApply unit testing, static code analysis, and other industry best practices for safety‑critical software /li liSupport integration testing, debugging, and root cause analysis of issues arising in system‑level testing (e.g., HIL/SIL) /li liDevelop and maintain technical documentation, including software design, implementation details, and traceability to requirements /li liContribute to continuous improvement of development processes, toolchains, and testing frameworks /li /ul h3Skills and Experiences /h3 ul liBachelor’s or Master’s degree in Electronics, Computer Engineering, Embedded Systems, or a related field /li liSome years of experience in embedded firmware development, preferably in medical or other regulated industries /li liExperience in developing firmware for microcontrollers (e.g., STM32, NXP, Renesas) in a real‑time environment /li liKnowledge of regulatory and quality requirements for medical device development is an advantage /li liStrong programming skills in C/C++, with experience in real‑time embedded firmware development /li liFamiliarity with RTOS platforms (e.g., Keil FuSa RTX, FreeRTOS, Zephyr, or similar) /li liExperience with low‑level hardware interfaces (e.g., SPI, I2C, UART, ADC/DAC, PWM, GPIO) /li liKnowledge of software development for safety‑critical systems, preferably in compliance with IEC 62304, ISO 13485, and ISO 14971 /li liExperience with unit testing, static analysis tools (e.g., Polyspace, Vectorcast, Cppcheck, PC‑lint, Coverity), and code coverage analysis /li liFamiliarity with version control (e.g., Git), issue tracking, and CI/CD pipelines for embedded projects /li liUnderstanding of CAN protocols, digital I/O, and embedded debugging tools (e.g., oscilloscopes, logic analyzers, JTAG/SWD) /li liBasic knowledge of hardware schematics and datasheets is a plus /li liStrong problem‑solving and analytical skills /li liGood communication skills and ability to work in cross‑functional teams /li liProactive, detail‑oriented, and committed to producing high‑quality and maintainable code /li liComfortable working in a regulated environment with structured development processes /li liOccasional travel may be required /li /ul h3What We Can Offer You /h3 ul liA dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth /li liExposure to a State‑of‑the‑Art medical device development process, in close cooperation with international clinicians /li liCompetitive base salary /li liVariable short‑term long‑term incentives /li liRecognition: through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements /li /ul pIf 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! /p pbWelcome to impact. Welcome to innovation. Welcome to your new life. /b /p /p #J-18808-Ljbffr

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