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Medical Device Professional for AI Training [Remote]

Remote, USA Full-time Posted 2026-06-13

Role Overview Join an innovative initiative to create realistic enterprise environments for training and evaluating frontier AI agents. As a Medical Devices Expert, you will leverage your experience from leading Fortune 500 medical device manufacturers to develop high-fidelity digital workspaces that reflect the complexities of regulated medical-device enterprises. Your expertise will be crucial in designing tasks that challenge state-of-the-art AI systems.

Key Responsibilities

  • Construct a realistic digital workspace based on your daily Drive folders, including design history files, regulatory submissions, risk-analysis matrices, and validation protocols, while incorporating relevant platforms like ANSYS Fluent and Siemens Opcenter.
  • Develop multi-step tasks rooted in your actual workflows, requiring navigation through various applications, files, and stakeholders to effectively challenge frontier AI agents.
  • Collaborate with fellow medical-device experts to design the environment, define task scope, and review scenarios for realism and rigor.
  • Engage asynchronously with research teams to refine task designs and establish evaluation criteria for medical-device agent benchmarks.
  • Contribute to pioneering AI research and benchmarking, with your work directly influencing how leading labs train and evaluate the next generation of AI systems.

Ideal Qualifications

  • Minimum of 3 years of full-time experience at a Fortune 500 medical-device manufacturer or large Tier-1 contract developer/manufacturer.
  • Expertise in one or more areas such as:
  • Regulatory affairs (510(k), PMA, De Novo, EU MDR, technical files)
  • Quality engineering/eQMS under 21 CFR 820, ISO 13485, ISO 14971
  • R&D or design controls (software-of-a-medical-device/SaMD is a plus)
  • Manufacturing engineering, process validation, or supplier quality
  • Clinical affairs, post-market surveillance, MDR/vigilance reporting
  • Relevant certifications are a plus: RAC, ASQ CQE/CRE/CBA.
  • Familiarity with ANSYS Fluent/STAR-CCM+, Siemens Opcenter or Rockwell FactoryTalk, and DocuSign.
  • Strong analytical thinking and writing skills, with the ability to translate regulated-device workflows into structured task specifications.

Compensation

Note

  • Task Completion Pay: Competitive, based on task quality (~$900, $1, 250 per completed task, subject to change as the project evolves).
  • Performance Bonus: Top performers receive a weekly bonus incentive in addition to their per-task rate.
  • Hourly Opportunity: Top performers may be invited to transition to an hourly compensation model based on sustained quality and throughput.

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