Senior Electrical Engineer

IPG Photonics•Marlborough, MA

About The Position

We are seeking a Senior Electrical Engineer to support the design and development of innovative medical device systems. The role covers embedded firmware development, circuit design, FPGA development, verification, regulatory compliance, and manufacturing transfer throughout the product development lifecycle.

Requirements

  • Bachelor's degree in Electrical Engineering.
  • At least 5 years of hardware and embedded firmware development experience, including product development in an ISO 13485-compliant medical device environment.
  • Experience with schematic capture and PCB design using OrCAD and/or Altium.
  • Strong analog and digital circuit design experience, including MCU- and FPGA-based systems.
  • Experience developing FPGA solutions using Verilog and embedded firmware for MCU-based systems using C.
  • Experience with hardware debugging, board bring-up, and root-cause analysis.
  • Experience with SPI, I2C, CAN, RS232, Ethernet, Wi-Fi, and Bluetooth communications.
  • Experience creating medical device design documentation, including requirements, design specifications, risk analysis, verification protocols, and reports.
  • Experience supporting manufacturing transfer, test fixture development, and production test procedures.
  • Strong communication, analytical, and problem-solving skills.
  • Self-motivated, with the ability to manage multiple projects in a fast-paced environment.

Nice To Haves

  • Master's degree in Electrical Engineering.
  • Experience with Quartus Prime and Keil development tools.
  • Experience with medical device compliance testing, including IEC 60601-1 and IEC 60601-1-2.
  • Experience with EMC troubleshooting and mitigation.

Responsibilities

  • Support the design and development of medical device systems.
  • Develop embedded firmware and FPGA solutions.
  • Design analog and digital circuits, including MCU- and FPGA-based systems.
  • Perform hardware debugging, board bring-up, and root-cause analysis.
  • Create medical device design documentation, including requirements, design specifications, risk analysis, verification protocols, and reports.
  • Support regulatory compliance and verification activities.
  • Support manufacturing transfer, test fixture development, and production test procedures.
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