Electronic Software Engineer
Il y a 7 mois
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 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
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
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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