Назад
Company hidden
4 дня назад

Technical Program Manager, AI Medical Devices

150 000 - 175 000
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US/Canada
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
Technical Program Manager, AI Medical Devices (AI medical devices): Coordinating end-to-end AI-enabled medical-device programs from product and model development through validation, regulatory readiness, launch, and post-market activities with an accent on cross-functional execution, design controls, and compliance. Focus on integrating AI/ML development, systems engineering, clinical validation, quality processes, and risk management across complex regulated programs.

Location: Remote, Canada. Applicants must be legally authorized to work in Canada or the USA and must not require current or future visa sponsorship.

Base salary: 150,000–175,000 in local currency per year, depending on experience and geographic location.

Company

hirify.global develops whole-body MRI scanning services and AI-enabled medical devices to support proactive healthcare.

What you will do

  • Coordinate planning, scheduling, milestone tracking, and execution across multiple AI-enabled medical-device programs.
  • Align AI/ML, software, systems engineering, product, regulatory, quality, clinical, and other teams.
  • Maintain project documentation and delivery tracking in Jira and related tools.
  • Coordinate design-control reviews and keep regulatory and quality deliverables current.
  • Support regulatory submission readiness, including 510(k), IDE, and Health Canada activities.
  • Report program status, risks, dependencies, and follow-ups while improving delivery processes.

Requirements

  • 5+ years of experience in technical program or project management, engineering program management, medical-device development, or a related field.
  • 2+ years of experience with regulated medical devices, Software as a Medical Device, digital health, or regulated clinical technology.
  • Experience coordinating multidisciplinary programs from development through verification, validation, and launch.
  • Technical fluency across software engineering, systems engineering, AI/ML research, and technical product development.
  • Understanding of datasets, model performance, validation, inference, deployment, and production monitoring.
  • Knowledge of design controls, risk management, verification and validation, change control, post-market processes, and FDA or Health Canada requirements.

Nice to have

  • Familiarity with ISO 13485, ISO 14971, and IEC 62304.
  • Experience with AI/ML-enabled medical devices or SaMD.
  • Experience coordinating clinical validation or clinical-performance evaluation.
  • Strong program planning, dependency management, risk management, and communication skills.
  • Comfort working in a fast-moving environment where scalable processes are still being established.

Culture & Benefits

  • Mission focused on preventive healthcare and positive patient impact.
  • Whole-body scans included as an employee benefit.
  • Growth opportunities and flexible career development.
  • Weekly team connection and social activities.
  • Flexible vacation policy.
  • Comprehensive health, dental, vision, and mental-health coverage; eligible Canadian employees can access RRSP and TFSA savings plans.

Hiring process

  • Successful candidates undergo a background check in compliance with applicable federal, provincial, and state rules.

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