Description
Willow is hiring an experienced Program Manager to lead new product introduction for connected medical devices. The role manages cross-functional programs from concept through design, verification and validation, transfer to manufacturing, and sustaining; coordinates hardware, firmware, software, regulatory, quality, clinical, and manufacturing teams; manages program risk, schedules, design controls, and phase-gate deliverables; and supports manufacturing readiness. The position requires 12+ years of experience, including 5+ years in program or project management for medical devices or regulated hardware or software, along with knowledge of FDA QSR, ISO 13485, IEC 62304, and ISO 14971.
