Senior Hardware Engineer – Medical Devices

Egnite HR TECH; Village of Tarrytown (NY); On-site; USD 110,000 - 170,000; Full time

Job summary

Egnite HR TECH is seeking an experienced hardware design professional for medical devices in the United States. The role focuses on leading hardware development, regulatory compliance, and sustaining engineering for regulated devices.

The candidate should have 7-8 years in medical device hardware, strong PCB/firmware interface knowledge, and hands-on risk management with standards like IEC 60601-1, ISO 14971, and ISO 13485. Collaboration with multi-disciplinary teams is essential.

Qualifications

• 7-8 years of experience in Medical Device Hardware Development.
• Experience with signal integrity techniques and layout constraints.
• MCU, FPGA, Sensor Interface Design
• Power Electronics, Battery-Powered Devices, DC-DC Converters
• High-Speed PCB Design (Ethernet, USB, SPI, I2C, CAN)
• PCB Design, DFM, DFT, SI/PI Analysis
• Hardware Verification & Validation (V&V)
• Hands on risk Management.
• IEC 60601-1, IEC 60601-1-2, ISO 14971, ISO 13485
• Windchill / Agile PLM
• Interfaces: USB, I2C, SPI, RS232, Ethernet, GSM, Bluetooth, Altium, OrCAD

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.

Job description

• 7-8 years of experience in Medical Device Hardware Development
• Analog, Digital & Mixed-Signal Design,
• Experience with signal integrity techniques and layout constraints.
• MCU, FPGA, Sensor Interface Design
• Power Electronics, Battery-Powered Devices, DC-DC Converters
• High-Speed PCB Design (Ethernet, USB, SPI, I2C, CAN)
• PCB Design, DFM, DFT, SI/PI Analysis
• Hardware Verification & Validation (V&V)
• Hands on risk Management.
• IEC 60601-1, IEC 60601-1-2, ISO 14971, ISO 13485
• Windchill / Agile PLM
• Interfaces: USB, I2C, SPI, RS232, Ethernet, GSM, Bluetooth, Altium, OrCAD

Preferred Skills

• Prior experience designing medical equipment or IVD systems.
• Experience with motion control systems, motor drivers, and precision sensors.

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.