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Posted May 25, 2026

Medical Device Professional for AI Training [Remote]

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.