Tarrytown, New York
β’
Today
Key Responsibilities Lead hardware design, development, and sustaining engineering activities for regulated medical devices.Perform schematic reviews, component selection, PCB design reviews, and hardware validation.Execute risk assessments, V&V, compliance testing, and regulatory support activities.Support manufacturing transfers, supplier changes, and cost optimization programs.Collaborate with Systems, Firmware, Mechanical, Quality, Regulatory, and Manufacturing teams.Must-Have Skills 10/15 y
Easy Apply
Contract, Third Party
Depends on Experience



