(Senior) Systems Engineering Consultant (m/f/d)
Adaptyx Biosciences - Menlo Park
Work at Adaptyx Biosciences
Overview
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Overview
We are looking for passionate, talented, and hardworking individuals to join our innovative team and help realize our vision.
Adaptyx Biosciences is seeking a Senior Embedded Systems Engineer to lead the firmware/software (FW/SW) development of our wearable continuous molecular monitoring device as we prototype towards our first product. This role focuses on designing, prototyping, and optimizing embedded systems for low-power, wearable biosensors that integrate seamlessly with our proprietary molecular sensing platform. As a key team member, you will collaborate with cross-disciplinary scientists and engineers to create high-performance embedded solutions, ensuring robust integration of hardware, firmware, and software.
Lead the design, development, and prototyping of FW/SW systems for our wearable biosensor platform.
Collaborate with hardware and software teams to integrate molecular sensing components into a compact, low-power wearable platform.
Develop firmware for microcontrollers and low-power SoCs to support sensor operation and data acquisition.
Develop software applications for interfacing with the biosensor system.
Conduct hardware testing, debugging, and performance tuning to optimize system reliability and accuracy.
Bluetooth, BLE, or similar) to transmit real-time data to companion devices.
BS/MS in Electrical Engineering, Computer Engineering, or related field.
~Proficiency in C/C++ for embedded firmware development and Python for data analysis and hardware validation.
~ Strong understanding of hardware-software integration and experience with microcontroller platforms (e.g., Proficiency in software development for data analysis and visualization (e.g. scripts, databases, PC applications, web applications, etc.).
~ Proficiency in bringing up, debugging and testing embedded hardware using tools like oscilloscopes, etc.
~ Knowledge of analog front-end design for sensor integration.
Experience developing hardware and/or FW/SW for medical devices in compliance with regulatory standards (e.g., Familiarity with Design Control processes, including requirements management, risk analysis (e.g., FMEA), and verification/validation testing.