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11 часов назад

Senior Field Clinical 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

Текст:
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TL;DR
Senior Field Clinical Engineer (Medical Devices): Supporting implantable spinal cord stimulation devices through clinical trials, field technical services, physician training, and product development with an accent on clinical research, patient safety, and device troubleshooting. Focus on coordinating IDE studies, resolving complex field issues, refining clinical protocols, and mentoring junior Field Clinical Engineers.

Location: California, United States

Company

hirify.global develops medical technologies and surgical solutions for patients with musculoskeletal disorders.

What you will do

  • Support feasibility studies, IDE clinical trials, post-market studies, and clinical site activities for spinal cord stimulation systems.
  • Coordinate patient fitting, interviewing, data collection, procedures, scheduling, and follow-up documentation.
  • Provide clinical device feedback, conduct product testing, and recommend design improvements and product iterations.
  • Train physicians, clinical staff, and sales team members on programming methods, clinical protocols, and technology utilization.
  • Troubleshoot complex field technical issues, document findings, and collaborate with Product Development and Quality Assurance on resolution.
  • Mentor junior Field Clinical Engineers and support clinical publications, presentations, marketing reviews, and sales programs.

Requirements

  • Bachelor’s degree in Engineering, Life Sciences, or a related technical field.
  • Minimum 6 years of field experience supporting implantable medical devices; 8 or more years preferred with a master’s degree or PhD.
  • Knowledge of human physiology, neuroanatomy, physician and hospital practices, and operating room etiquette.
  • Experience conducting IDE clinical trials, applying GCP principles, and following regulatory requirements.
  • Strong communication, critical-thinking, problem-solving, organizational, and documentation skills, with proficiency in Microsoft Office.
  • Ability to travel 50–70% of the time, including overnight and weekend travel.

Culture & Benefits

  • Work guided by innovation, customer focus, teamwork, and results-driven execution.
  • Emphasis on patient care, ethical conduct, regulatory compliance, and scientific excellence.
  • Equal employment opportunity and an inclusive, respectful workplace.

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