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Mercor

Cincinnatus is an enterprise staffing company that partners with leading technology companies to source and employ highly skilled professionals for full-time and long-term contingent roles. Cincinnatus serves as the employer of record for these engagements, providing W-2 employment, payroll, benefits, and compliance, while placing employees directly within client teams to work on high-impact initiatives. Roles hired through Cincinnatus are not project-based or freelance engagements. They are structured, role-based positions that typically involve full-time or fixed-term commitments, close collaboration with a client's internal teams, and integration into standard enterprise workflows. Cincinnatus is a legal entity separate from Mercor. While opportunities may be discovered through Mercor's platform, employment, onboarding, payroll, and benefits for these roles are administered by Cincinnatus. Equal Employment Opportunity Cincinnatus is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, reproductive health decisions, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetic information, political views or activity, or any other legally protected characteristic. Cincinnatus is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans throughout the job application process.

Medical Device R&D Specialist

Research AnalystResearch AnalystPart TimeRemoteMid LevelH1B No Sponsor

Location

United States

Posted

25 days ago

Salary

$1.2K - $1.5K / year

Seniority

Mid Level

No structured requirement data.

Job Description

Medical Device R&D Specialist

Mercor

Role Description - Build a realistic digital workspace centered on the Drive folders you use day-to-day, including: - Design history files - Regulatory submissions - DHF/DMR documents - Risk-analysis matrices - Validation protocols - CAPA records - Email threads - Represent platforms like ANSYS Fluent, Siemens Opcenter MES, and DocuSign. - Design multi-step tasks grounded in your real workflows, requiring navigation of multiple apps, files, and stakeholders to challenge frontier AI agents. - Collaborate with other medical-device experts to: - Design the environment - Shape task scope - Review scenarios for realism and rigor - Work asynchronously with research teams to refine task designs and evaluation criteria for medical-device agent benchmarks. - Contribute to frontier AI research and benchmarking, directly informing how leading labs train and evaluate the next generation of AI systems. Qualifications - Must-Have: - 3+ years of full-time experience at a Fortune 500 medical-device manufacturer or large Tier-1 contract developer/manufacturer. - Background in regulatory affairs, quality engineering, R&D, manufacturing engineering, or clinical affairs. - Day-to-day use of ANSYS Fluent, Siemens Opcenter, or DocuSign. - Strong analytical thinking and writing skills. - Preferred Certifications: - RAC - ASQ CQE/CRE/CBA Requirements - Task Completion Pay: Competitive and based on task quality (~$1,150–$1,450 per completed task). - Performance Bonus: Weekly bonus incentive for top performers. - Hourly Opportunity: Transition to hourly compensation based on sustained quality and throughput. Application Process - Upload resume - AI interview based on your resume - Submit form Resources & Support - For details about the interview process and platform information, please check: Interview Process - For any help or support, reach out to: support@mercor.com - Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

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