About the company
Beacon Biosignals is transforming precision medicine for the brain, from clinical development to clinical care. For Life Sciences partners, we offer the leading at-home EEG platform for clinical development of novel therapeutics for neurological, psychiatric, and sleep disorders. Our Diagnostics business is building the most comprehensive at-home platform for precision diagnostics, combining EEG and cardiopulmonary signals to deliver reimbursable assessments for sleep and central nervous system disorders.
Responsibilities
- Develop and execute device testing in accordance with Beacon’s QMS.
- Develop and document test plans, test protocols, and test scripts for embedded systems, including hardware, firmware, and software, based on design specifications and requirements.
- Develop and maintain test procedures, fixtures, and equipment.
- Conduct functional, integration, system, and regression testing on hardware and firmware.
- Work closely with hardware and firmware engineers to troubleshoot and resolve product issues.
- Ensure products meet industry standards, safety, and regulatory requirements (e.g., FDA, CE, 60601).
- Implement process improvements and test automation to enhance product quality and testing efficiency.
Requirements
- Education: BS in engineering or related field.
- Work Experience (post-graduate): 5+ years of professional engineering experience with a BS degree or 3+ years of professional engineering experience with an MS degree or above.
- Experience with writing detailed technical specifications and documentation, including requirements, test plans, protocols, and reports.
- Ability to read and follow electrical schematics.
- Experience with embedded software that runs on a real-time operating system (RTOS).
- Experience with scripting languages such as Python.
- Experience with troubleshooting, debugging, and root cause analysis of hardware and firmware issues in electromechanical systems.
- Experience with tools like Git/JIRA and platforms like GitHub.
- Preferably, knowledge of design controls and regulations for medical devices.
Conditions
- This role is required to work from the Boston office on average approximately 3 days per week with flexible days and hours.
- The salary range for this role is $120,000 – $140,000.
- The base salary is one component of the total compensation package, which includes equity, PTO and other benefits.