Electronic Software Engineer
il y a 2 jours
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 missionsPosition 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 systemConduct feasibility studies, design software tools to inform the design and development processCollaborate with electronic and mechanical engineers to integrate components and systems, optimizing functionality and performanceDevelop with the electronic engineers the firmware which have to drive the hardware resource in the implanted device and to communicate with the external devicesDefine the software architecture of the deviceDefine the software design specificationsDefine the software test strategy and drive the tests to evaluate the performance, reliability, and safety of implant prototypesVos compétencesQualifications:Bachelor’s degree or higher in technical education, or equivalent, with a focus on software engineering ; Master’s degree preferredFamiliarity with standard project management tools and design controls for medical devices or a similarly regulated industryMinimum 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 plusKnowledge 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 environmentExperience in BLE communicationExperience with test method development, testing, and validation of test methods. Strong understanding of medical device design principles, materials science, and manufacturing processesEffective communication skills and the ability to work effectively in a cross-functional team environmentFluency in English; French language proficiency is a plusAvantagesBenefits:Competitive salary and equity optionsFlexible work scheduleProfessional development opportunitiesCollaborative and inclusive work cultureJoin 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 #J-18808-Ljbffr
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