What You Will Do

Define and maintain physical product design standards for all Hike-fabricated devices (custom inserts, AFOs, and future categories).
Review design outputs from the fabrication team for clinical appropriateness and set quality gates before devices ship.
Build and maintain the physical product roadmap: what improvements are needed, in what sequence, and why.
Define the biomechanical rationale for device selection criteria in Hike Clinical evaluation modules.
Track device outcome data and incorporate learnings into design standards.
Evaluate third-party manufacturing partners for prefabricated categories against Hike quality standards.
Support clinical protocols with biomechanical expertise, particularly for custom AFO and prosthetic categories.

What We Are Looking For

Degree in biomechanics, biomedical engineering, orthotics & prosthetics, physical therapy, or a related clinical/engineering field.
3+ years in lower-extremity device design or clinical biomechanics, preferably in manufacturing or an O&P practice.
Hands-on knowledge of AFO design mechanics: rigid vs. articulated, ground reaction force AFOs, floor reaction configurations, and SMO indications.
Experience evaluating prefabricated device options against clinical standards.
Ability to communicate biomechanical rationale in plain language for protocols and documentation.
Familiarity with 3D scanning, CAD, and/or additive manufacturing for custom devices a strong plus.