Jobs at LifeLens Technologies

Develop and validate biomedical signal-processing algorithms for wearable devices using PPG, ECG, accelerometry, and other sensors. Analyze clinical and field datasets, address motion artifacts, adapt algorithms for real-time embedded implementation, and design validation studies. Produce verification and regulatory submission documentation, write reproducible code, collaborate with hardware, firmware, and clinical teams, communicate technical findings, and mentor junior team members.

Develop and validate signal-processing algorithms for wearable health devices using PPG, ECG, and accelerometer data. Analyze clinical and field datasets, address motion artifacts, build data-processing pipelines, adapt algorithms for real-time device use, and support clinical validation and regulatory documentation. Collaborate with hardware, firmware, clinical, and engineering teams while producing tested, reproducible code and communicating technical findings.

Designs, debugs, verifies, and documents electrical hardware for wearable medical devices. Responsibilities include schematic and PCB development, BOM creation, RF and antenna design, power management, manufacturing transfer, testing, certification, electrical safety, EMC compliance, RoHS compliance, and hardware improvement projects. The role collaborates with contract manufacturers, certification laboratories, and internal engineering and manufacturing teams.

Performs manual and automated software, hardware, and firmware testing across smoke, regression, integration, and end-to-end scenarios. Creates test plans, procedures, and cases; analyzes results; documents defects; reviews requirements and designs; collaborates with developers; and manages testing timelines and documentation. The role is full-time and on-site, with up to 25% customer travel.

Develops electrochemical medical devices from concept through regulatory clearance and commercialization. Responsibilities include prototyping, performance evaluation, design selection, risk management, design documentation, verification and validation testing, manufacturing support, and collaboration with manufacturing, quality, and regulatory teams. The role requires experience with Class II or III medical devices, Design Controls, international standards, experimental methods, prototyping, material characterization, and manufacturing equipment qualification.

Leads process development, validation, risk analysis, and continuous improvement for medical device manufacturing. Develops and validates stable production processes, conducts trials and DOE studies, evaluates materials and process changes, establishes acceptance criteria, and authors technical reports. Collaborates with Quality, R&D, engineers, and technicians while supporting manufacturing operations, implementing equipment safety protocols, and leading process improvement initiatives.