Electronic Software Engineer

il y a 5 jours


Paris, Île-de-France EDUCAT Temps plein
About EDUCAT

We are a dynamic and innovative start-up based in Paris, focused on the development of novel active implant technologies aimed at revolutionizing healthcare solutions. Our team of 15 highly skilled professionals is committed to pushing the boundaries of medical technology to improve patient outcomes and quality of life.

Job 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 lead the development of 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.

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 has 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
Requirements
  • 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)
  • 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
What We Offer
  • Competitive salary and equity options
  • Flexible work schedule
  • Professional development opportunities
  • Collaborative and inclusive work culture


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