Technical Program Manager, AI Medical Devices
Prenuvo · Remote, Canada
Posted 20 days ago · $150,000-$175,000
or apply directly on Prenuvo's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 20 days Prenuvo's roles stay open a median of 23 days
- Reposted
- No
- Salary listed
- Yes 84% of Prenuvo's roles list one
- Ghost-job risk at Prenuvo
- moderate 10 stale, 1 reposted of 49 open
- Hiring momentum
- 77 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Prenuvo's own greenhouse board since 2026-08-03. Full hiring picture for Prenuvo.
About this role
As a Technical Program Manager for AI Medical Devices at Prenuvo, you will coordinate the execution of AI-enabled medical-device programs, collaborating with various teams including AI Research, Engineering, and Regulatory Affairs. Your role involves managing project planning, documentation, and compliance, while ensuring effective communication and alignment across multidisciplinary teams to enhance product development and delivery efficiency.
- benefits
- 2/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Prenuvo as an employer.
What you need
- 5+ years of experience in Technical Program Management, Technical Project Management, Engineering Program Management, medical-device product development, or a closely related discipline
- 2+ years working with regulated medical devices, Software as a Medical Device, digital health, or similarly regulated clinical technology
- Experience coordinating multidisciplinary technical programs from development through verification/validation and launch
- Strong technical fluency and the ability to work credibly with software engineers, systems engineers, AI/ML researchers, and technical product leaders
- Familiarity with machine-learning development concepts such as datasets, model performance, validation, inference, deployment, and production monitoring
- Working knowledge of regulated medical-device development practices, including design controls, risk management, verification and validation, change control, and post-market processes
Nice to have
- Familiarity with standards such as ISO 13485, ISO 14971, and IEC 62304
- Experience specifically with AI/ML-enabled medical devices or SaMD
- Experience coordinating clinical validation or clinical-performance evaluation
- Excellent program-planning, dependency-management, and risk-management skills
- Exceptional communication and the ability to create clarity across specialized technical disciplines
What you get
- Whole-body scans as part of employee benefits
- Flexible vacation policy
- Comprehensive benefits package including health, dental, vision, and Mental Health coverage
- Access to RRSP and TFSA retirement savings plans with immediate, optional enrollment
Worth weighing
- No visa sponsorship provided; applicants must be authorized to work in Canada or the USA
- Salary range is specified but may vary based on experience and location
- The role involves working in a fast-paced environment where processes are still being developed
Summarised from Prenuvo's posting. Read the full original.
Listed by Prenuvo on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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