Electronic Software Engineer
il y a 6 heures
Company Overview: We are a dynamic and innovative start-up based in Paris, focused on the development of a novel active implant aimed at revolutionizing healthcare solutions. With a team of 15 highly skilled professionals today (to be increased up to around 35 in 2024+2025), we are committed to pushing the boundaries of medical technology to improve patient outcomes and quality of life. Vos missions Position Overview: As a software Engineer, you will be an integral part of our R&D team, contributing your expertise to the design, development, and optimization of our innovative active implant technology. You will be leading the development of a firmware in the implanted system and collaborate closely with the cross-functional team (R&D, Quality, Regulatory). This is a unique opportunity to join a fast-paced start-up environment and make a meaningful impact on the future of healthcare. This is a full-time opportunity and requires willingness to relocate to Paris, France. Key Responsibilities: Lead and drive the embedded software project according to the software development cycle on a critical sub-system of an active implant system Conduct feasibility studies, design software tools to inform the design and development process Collaborate with electronic and mechanical engineers to integrate components and systems, optimizing functionality and performance Develop with the electronic engineers the firmware which have to drive the hardware resource in the implanted device and to communicate with the external devices Define the software architecture of the device Define the software design specifications Define the software test strategy and drive the tests to evaluate the performance, reliability, and safety of implant prototypes Vos compétences Qualifications: Bachelor’s degree or higher in technical education, or equivalent, with a focus on software engineering ; Master’s degree preferred Familiarity with standard project management tools and design controls for medical devices or a similarly regulated industry Minimum of 5 years of experience in research and development, preferably within the Class III implantable technology industry (e.g., ISO 13485, FDA QSR) is a plus Knowledge of medical devices standards and regulations in particular for Active Implantable Medical Devices (IEC 62304) Experience in embedded software development such as STM32xx or NORDIC nRFxx environment Experience in BLE communication Experience with test method development, testing, and validation of test methods. Strong understanding of medical device design principles, materials science, and manufacturing processes Effective communication skills and the ability to work effectively in a cross-functional team environment Fluency in English; French language proficiency is a plus Avantages Benefits: Competitive salary and equity options Flexible work schedule Professional development opportunities Collaborative and inclusive work culture Join us in our mission to transform healthcare through innovation and make a difference in the lives of patients worldwide. Apply now to be a part of our passionate and dedicated team
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