Senior Electrical Engineer

IPG Photonics•Marlborough, MA

About The Position

The Senior Electrical Engineer supports the design and development of innovative medical device systems throughout the product development lifecycle. The role encompasses embedded firmware development, circuit design, FPGA development, verification, regulatory compliance, and manufacturing transfer.

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

  • Develop embedded firmware for MCU-based systems using C.
  • Design analog and digital circuits, including systems based on MCUs and FPGAs.
  • Develop FPGA solutions using Verilog.
  • 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 manufacturing transfer, test fixture development, and production test procedures.
  • Support verification and regulatory compliance throughout product development.
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