Firmware Engineer (Medical Device)
About Us
Your Role
Reporting directly to the CTO, you will play a key role in developing the firmware and back-end systems that power our innovative products. This is a hands-on engineering role with the opportunity to influence the design and implementation of mission-critical technology.
Responsibilities
- Develop and optimize firmware for our neurotech devices, ensuring seamless performance and reliability.
- Build and maintain robust back-end services to support device monitoring, data processing, and system interactions.
- Design systems for monitoring device health and managing interactions between cloud-based services and embedded devices.
- Conduct code reviews, design reviews, and risk analyses.
- Develop test plans and prepare comprehensive test reports.
- Ensure compliance with ISO13485 standards and adhere to best practices in the medical device industry.
- Collaborate with a cross-functional team of engineers, designers, and researchers to deliver impactful solutions.
What We’re Looking For
Required Qualifications
- Strong proficiency in C++, preferably in an embedded systems context.
- Hands-on experience with embedded systems and firmware development.
- Bachelor’s degree in Computer Science, Software Engineering, Mechatronics, Electrical Engineering, or a related field — or equivalent professional experience.
Desirable Experience
- Experience with Rust is highly desirable. Alternatively, an eagerness to learn Rust is essential.
- Strong understanding of modern C++ practices and norms.
- Experience working in real-time systems with an RTOS. Particularly nRF Connect SDK and Zephyr is a bonus.
- Familiarity with Bluetooth Low Energy (BLE).
- Knowledge of cloud platforms and frameworks such as Firebase or Google Cloud.
- Background in medical device software development and familiarity with regulatory environments, such as ISO13485, IEC62304, FDA, or CE.
The Ideal Candidate
- You're meticulous, driven, and committed to building technology that makes a real difference.
- You handle the pace of a startup well and tackle complex problems with enthusiasm.
- You're keen to learn, particularly about medical device standards, and prepared to evolve alongside our company.
Why Join Us?
- Impact: Be part of a mission-driven team working to improve health and well-being on a global scale.
- Growth: Receive hands-on training in medical device standards and regulatory compliance, while honing your technical skills.
- Opportunity: Work with a team of seasoned professionals who have deep experience in startups, deep-tech, and a successful exit.
- Rewards: Enjoy significant potential for financial rewards as an early team member.
To Apply:
Please send an introductory letter and copy of your CV in pdf format to hr[at]affectablesleep.com
No Recruiters: We kindly ask that recruitment agencies do not respond to this advertisement.
Location Preference: We prefer applicants based in or willing to move to Sydney, Australia.
Compensation: Compensation will be based on experience.
We are an equal opportunity employer and welcome applications from all qualified candidates regardless of race, color, religion, sex, national origin, age, disability, or any other characteristic protected by law.
Your personal information will be used solely for the purposes of this recruitment process and will be kept confidential.
