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обновлено 11 дней назад

Enabling Technologies Technical Lead (Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Enabling Technologies Technical Lead (Medical Devices): Leading the design, development, and commercialization of orthopedic medical device technologies spanning software, algorithms, electronics, mechanical systems, instrumentation, and visualization with an accent on system architecture, regulatory compliance, and multidisciplinary technical execution. Focus on integrating computer vision, sensor fusion, navigation, image processing, automation, and augmented reality while managing technical risks and supporting verification, validation, and design transfer.

Location: Austin, Texas, United States. Full-time work authorization in the United States is required; visa sponsorship is not available. Minimal to moderate business travel may be required.

Company

hirify.global is a medical technology company developing clinically differentiated orthopedic solutions, integrated technologies, and products designed to improve patient outcomes and transform clinical workflows.

What you will do

  • Provide technical leadership across multidisciplinary medical device programs from concept through commercialization.
  • Define system architecture and integrate hardware, software, sensors, optics, visualization, instrumentation, and enabling technologies.
  • Lead design reviews covering software, embedded systems, algorithms, electronics, mechanical design, manufacturability, usability, and clinical workflow.
  • Drive development of navigation, visualization, computer vision, sensor fusion, image processing, automation, and related orthopedic technologies.
  • Identify technical risks and support verification, validation, usability engineering, design transfer, and regulatory compliance.
  • Mentor engineering teams and drive technology roadmaps, invention disclosures, patents, and continuous improvement.

Requirements

  • Bachelor’s degree in engineering, computer science, software engineering, electrical engineering, biomedical engineering, or a related technical discipline; a master’s degree is preferred.
  • At least 7 years of experience developing complex medical devices or related technology products.
  • Experience leading multidisciplinary engineering teams and integrating software, electronics, mechanical systems, and algorithms.
  • Knowledge of medical device design controls, system architecture, technical risk management, verification and validation, and product lifecycle management.
  • Strong analytical, organizational, leadership, written, and verbal communication skills.
  • Must already have full-time work authorization in the United States without requiring current or future employment visa sponsorship. A valid passport must be held or obtainable for international business travel.

Nice to have

  • Experience with orthopedic navigation, visualization, image-guided surgery, computer vision, sensor fusion, inertial navigation, optical tracking, or image processing.
  • Experience with mechatronics, automation, advanced control systems, orthopedic instrumentation, or capital medical equipment.
  • Familiarity with IEC 62304, ISO 13485, ISO 14971, IEC 60601, FDA Design Controls, and EU MDR.
  • Experience commercializing Class II or Class III medical devices and leading multidisciplinary engineering organizations.
  • A patent portfolio or demonstrated history of technical innovation.

Culture & Benefits

  • Collaborative, multidisciplinary environment focused on scientific excellence, innovation, and continuous improvement.
  • Medical, dental, and vision insurance.
  • Spending and savings accounts, income protection plans, and a 401(k) plan.
  • Vacation, sick leave, holidays, discounted insurance rates, and legal services.

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