4 дня назад
Technical Program Manager, AI Medical Devices
150 000 - 175 000₽
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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