Technical Fellow, Medical Robotics & Systems Hardware

Magnendo Corp.

Newton (MA)

On-site

USD 260,000 - 350,000

Full time

14 days+

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Job summary

Magnendo Corp. in Massachusetts seeks a Technical Fellow to own hardware subsystems, UI/UX workflow requirements, and steerable guidewire design for its robotic endovascular platform.

You will work across hardware, software, and clinical teams to integrate designs under medical device standards. Qualifications include 13+ years in medical device robotics, hands-on hardware architecture, and experience with IEC 60601 and ISO 14971.

Qualifications

  • 13+ years of hands-on medical device engineering and robotics experience.
  • Experience owning systems-level hardware architecture across mechanical, electrical, and controls.
  • Experience applying medical device safety standards such as IEC 60601 and ISO 14971.
  • Experience defining procedural workflow and usability requirements informed by IEC 62366-1.
  • Portfolio of patents or tangible evidence of innovative technical contributions.

Responsibilities

  • Own systems engineering for hardware components of the platform (robot chassis, sensors, advancer unit) in line with medical standards.
  • Define requirements, architecture, and interfaces across hardware subsystems with multidisciplinary teams.
  • Partner with external hardware design teams to validate mechanical and electromechanical requirements.
  • Lead guidewire design from concept to prototyping in collaboration with contract manufacturers.
  • Support risk analysis, design reviews, and root-cause investigations per ISO 14971.

Skills

Systems engineering
Hardware architecture
UI/UX usability
Prototyping & testing
Medical device safety standards

Education

BS in Engineering
MS in Engineering
PhD in Engineering

Job description

Magnendo Corp. in Massachusetts seeks a Technical Fellow to own hardware subsystems, UI/UX workflow requirements, and steerable guidewire design for its robotic endovascular platform.

You will work across hardware, software, and clinical teams to integrate designs under medical device standards. Qualifications include 13+ years in medical device robotics, hands-on hardware architecture, and experience with IEC 60601 and ISO 14971.

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