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
ā¢ 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.
ā¢ Develop multi-step tasks rooted in your actual workflows, requiring navigation through various applications, files, and stakeholders to effectively challenge frontier AI agents.
ā¢ Collaborate with fellow medical-device experts to design the environment, define task scope, and review scenarios for realism and rigor.
ā¢ Engage asynchronously with research teams to refine task designs and establish evaluation criteria for medical-device agent benchmarks.
ā¢ 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
ā¢ Minimum of 3 years of full-time experience at a Fortune 500 medical-device manufacturer or large Tier-1 contract developer/manufacturer.
ā¢ Expertise in one or more areas such as:
ā¢ Regulatory affairs (510(k), PMA, De Novo, EU MDR, technical files)
ā¢ Quality engineering/eQMS under 21 CFR 820, ISO 13485, ISO 14971
ā¢ R&D or design controls (software-of-a-medical-device/SaMD is a plus)
ā¢ Manufacturing engineering, process validation, or supplier quality
ā¢ Clinical affairs, post-market surveillance, MDR/vigilance reporting
ā¢ Relevant certifications are a plus: RAC, ASQ CQE/CRE/CBA.
ā¢ Familiarity with ANSYS Fluent/STAR-CCM+, Siemens Opcenter or Rockwell FactoryTalk, and DocuSign.
ā¢ Strong analytical thinking and writing skills, with the ability to translate regulated-device workflows into structured task specifications.
Compensation Note
ā¢ Task Completion Pay: Competitive, based on task quality (~$900, $1, 250 per completed task, subject to change as the project evolves).
ā¢ Performance Bonus: Top performers receive a weekly bonus incentive in addition to their per-task rate.
ā¢ Hourly Opportunity: Top performers may be invited to transition to an hourly compensation model based on sustained quality and throughput.
Apply tot his job
Apply To this Job
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
ā¢ 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.
ā¢ Develop multi-step tasks rooted in your actual workflows, requiring navigation through various applications, files, and stakeholders to effectively challenge frontier AI agents.
ā¢ Collaborate with fellow medical-device experts to design the environment, define task scope, and review scenarios for realism and rigor.
ā¢ Engage asynchronously with research teams to refine task designs and establish evaluation criteria for medical-device agent benchmarks.
ā¢ 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
ā¢ Minimum of 3 years of full-time experience at a Fortune 500 medical-device manufacturer or large Tier-1 contract developer/manufacturer.
ā¢ Expertise in one or more areas such as:
ā¢ Regulatory affairs (510(k), PMA, De Novo, EU MDR, technical files)
ā¢ Quality engineering/eQMS under 21 CFR 820, ISO 13485, ISO 14971
ā¢ R&D or design controls (software-of-a-medical-device/SaMD is a plus)
ā¢ Manufacturing engineering, process validation, or supplier quality
ā¢ Clinical affairs, post-market surveillance, MDR/vigilance reporting
ā¢ Relevant certifications are a plus: RAC, ASQ CQE/CRE/CBA.
ā¢ Familiarity with ANSYS Fluent/STAR-CCM+, Siemens Opcenter or Rockwell FactoryTalk, and DocuSign.
ā¢ Strong analytical thinking and writing skills, with the ability to translate regulated-device workflows into structured task specifications.
Compensation Note
ā¢ Task Completion Pay: Competitive, based on task quality (~$900, $1, 250 per completed task, subject to change as the project evolves).
ā¢ Performance Bonus: Top performers receive a weekly bonus incentive in addition to their per-task rate.
ā¢ Hourly Opportunity: Top performers may be invited to transition to an hourly compensation model based on sustained quality and throughput.
Apply tot his job
Apply To this Job