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Fractional Wearables Lead

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Onsite

Fractional Wearables Lead

Stealth Startup

Fractional Wearables Lead

1 month ago

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Important information


Contract type:

Permanent

Location:

Chicago, IL, USA

Work mode:

Onsite

Published on:

21 September 2026

What they need


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.

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