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6 часов назад

Senior Electrical Engineer (Medical Devices)

Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

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TL;DR
Senior Electrical Engineer (Medical Devices): Leading the design and development of Class III implantable neuromodulation systems for spinal cord injury repair with an accent on embedded systems, mixed-signal electronics, power management, and medical-device compliance. Focus on shaping electrical architecture, validating hardware performance, mitigating design risks, and integrating electrical subsystems across multidisciplinary teams.

Location: Audubon, Pennsylvania, United States

Company

hirify.global develops medical technologies and evidence-based therapies for patients with musculoskeletal disorders.

What you will do

  • Lead the electrical design and development of Class III implantable neuromodulation systems, accessories, test systems, and manufacturing fixtures.
  • Design and analyze embedded, mixed-signal, analog, digital, power-management, and charging circuits.
  • Own schematics, PCB layouts, component selection, bills of materials, characterization, and system integration.
  • Establish electrical requirements, specifications, system constraints, and verification methods across the product lifecycle.
  • Lead cross-functional engineering activities, influence architecture and manufacturing decisions, and manage electrical risks.
  • Develop prototypes and investigational designs, support laboratory and clinical research, and contribute to intellectual property generation.

Requirements

  • Bachelor’s degree with 8 years, Master’s degree with 6 years, or PhD with 3 years of related medical-device development or verification experience.
  • At least 5 years of experience in a regulated industry; Class III medical-device experience is strongly preferred.
  • Advanced expertise in embedded systems, mixed-signal electronics, and power electronics.
  • Experience with FDA submission processes, ISO 13485, Quality System Regulation, and standards including 60601, 14708, 14971, and FCC.
  • Experience with C, Assembly, or Python for firmware guidance and hardware-characterization tools.
  • Ability to coordinate complex engineering programs, communicate across disciplines, and travel approximately 10% domestically and internationally.

Culture & Benefits

  • Work is guided by innovation, customer focus, teamwork, and results-oriented execution.
  • Collaboration with systems, mechanical, firmware, manufacturing, quality, regulatory, physicians, and clinicians.
  • Focus on patient safety, product reliability, ethical conduct, and compliance with applicable regulations.
  • Reasonable accommodations are available for individuals with disabilities.

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