Ceribell is a medical technology company focused on transforming the diagnosis and management of patients with serious neurological conditions. The Ceribell System is a novel, point-of-care electroencephalography (“EEG”) platform specifically designed to address the unmet needs of patients in the acute care setting.
Requirements
- Familiarity with signal acquisition tools (BioSemi, OpenBCI, g.tec, or similar)
- Experience collecting EEG data and the ability to verify data quality and integrity.
- Relevant experience in the development of medical device projects.
- Exposure to SolidWorks and Python or MATLAB.
- Experience with regulatory compliance testing
Responsibilities
- Set up and operate EEG recording systems for in-house and partner studies.
- Prepare electrodes, headgear, and participant workstations following study protocols
- Aid in the creation and effective execution of study protocols, data collection, and analysis.
- Create and perform test procedures to verify functionality, performance, and reliability.
- Generate reports and associated documentation for regulatory submissions.
- Assemble, test, and maintain hardware prototypes (EEG amplifiers, headgear, connectors, enclosures).
- Perform bench-level tests (signal integrity, timing, accuracy, power measurements) using oscilloscopes and DAQs)
Other
- On-site presence is required at Ceribell’s Sunnyvale office in California and is expected to last between 3 and 6 months.
- Bachelor’s Degree in Biomedical Engineering, Neuroscience, Neuroengineering, or other relevant field.
- 1-3 years of experience as a Biomedical engineer or relevant experience.
- Excellent verbal and written communication and strong problem-solving skills.
