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Stealth Startup

Fractional Wearables Lead

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Job Description

Fractional Wearables Lead at Stealth Startup Fractional Wearables Lead at Stealth Startup in Chicago, Illinois Posted in about 22 hours ago.
Type:
full-time
Job Description:
Job Description:
Fractional Wearables Lead Location:
Chicago, IL - Hybrid / On-site for lab testing
Type:
Fractional Contract /
Contract-to-Hire Target Start:
Immediate - Q3/Q4 2026 ??
CRITICAL GATEKEEPER
To save everyone's time, we are only considering candidates who have personally shipped a regulated medical wearable (Class II or Class III) through FDA clearance or CE Mark approval and have hands-on experience authoring
IEC 62366
usability engineering documentation. General consumer product design, non-regulated wearables, or pure software/cloud experience will not meet the technical requirements of this clinical hardware role. Role Overview We are seeking a highly specialized Fractional Wearables Lead to own the physical patient-to-device interface for our next-generation EEG wearable patch. This role will be critical to achieving medical-grade EEG signal integrity, reliable device performance, and patient comfort during continuous, multi-day wear.
Key Responsibilities Electrode & Materials Engineering:
Lead the selection and evaluation of medical-grade adhesives and wearable materials. Characterize and optimize skin-electrode impedance stability and develop solutions to minimize motion artifacts.
Mechanical & Form Factor Design:
Design, prototype, and iterate on wearable form factors, including patch and behind-the-ear configurations, while optimizing retention, comfort, and usability across diverse skin and hair types.
Human Factors & Usability:
Lead usability engineering activities in accordance with
IEC 62366
. Design intuitive donning and doffing workflows for patients and caregivers and author usability documentation for FDA and other regulatory submissions.
Cross-Functional Collaboration:
Work closely with electrical engineering, firmware, analog front-end, clinical, and regulatory teams. Support biocompatibility testing in accordance with ISO 10993 and contribute to regulatory submissions.
Clinical Build Support:
Support the assembly and testing of our first clinical-build wearable patch and contribute to the design of early clinical studies planned for late 2026. Hard Gatekeeper Requirements Candidates must meet all of the following requirements:
Regulated Medical Wearables:
Personally shipped at least one regulated Class II or Class III medical wearable -such as a
CGM, ECG/EEG
patch, or smart hearable-that successfully achieved FDA clearance or CE Mark approval .
Hands-On Usability Engineering:
Proven experience authoring
IEC 62366
usability engineering files/documentation for an actual regulatory submission.
Electrode & Adhesive Expertise:
Deep technical expertise in skin-electrode interface physics, impedance characterization/testing, motion-artifact mitigation, and medical adhesive behavior.
Hardware Engineering Experience:
Hands-on experience with the physical design, testing, prototyping, and validation of medical wearables.
Location & Availability:
Ability to support hardware testing and collaborate with our Chicago-based engineering lab as needed. This is a hands-on engineering role, not a high-level project management position. Candidates who do not meet the hard gatekeeper requirements above will not be considered.