Senior Embedded Firmware Engineer – Medical Devices

NML Medical

Methuen (MA)

On-site

USD 120,000 - 160,000

Full time

14 days+

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Job summary

Globus Medical in Methuen, MA is seeking a Staff Firmware Engineer to advance embedded software for medical devices. The role covers from concept through transfer to manufacturing and requires strong C/C++ skills and experience with ARM microcontrollers and RTOS.

You will work in a regulated setting, collaborate with cross‑functional teams, and help ensure system performance and compliance with FDA/ISO guidelines.

Qualifications

  • B.S. in Computer Engineering, Electrical Engineering, or similar degree.
  • 7-10 years of proven experience in software design for embedded systems.
  • Knowledge of C/C++ and embedded firmware development.Required.
  • Experience in high-reliability fields such as medical devices preferred.
  • Experience with hardware platforms and interpreting schematics.
  • Hands‑on experience with oscilloscopes, analyzers is required.
  • ARM MCUs and RTOS experience preferred; FDA/ISO knowledge preferred.

Responsibilities

  • Develops embedded bare-metal firmware interfacing with hardware and software platforms.
  • Support hardware integration across systems, debug issues and field returns.
  • Develop firmware in a regulated environment following SOPs and standards.
  • Self-directed planning and action to obtain results; communicate risks to management.
  • Coordinate significant engineering development efforts with internal and external teams.
  • Ensure interface compatibility and system performance with other components.

Skills

Embedded firmware
C/C++
ARM microcontrollers
RTOS
Hardware interaction

Education

B.S. in Computer Engineering or Electrical Engineering

Job description

Globus Medical in Methuen, MA is seeking a Staff Firmware Engineer to advance embedded software for medical devices. The role covers from concept through transfer to manufacturing and requires strong C/C++ skills and experience with ARM microcontrollers and RTOS.

You will work in a regulated setting, collaborate with cross‑functional teams, and help ensure system performance and compliance with FDA/ISO guidelines.

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