[Hiring] Senior Quality Engineer @Mercor

Role Description

• Build a realistic digital workspace centered on the Drive folders you use daily, including:
  • Design history files
  • Regulatory submissions
  • DHF/DMR documents
  • Risk-analysis matrices
  • Validation protocols
  • CAPA records
  • Email threads
• Design multi-step tasks grounded in real workflows, navigating 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, 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

• Project will transition from an hourly rate to compensation based on throughput of quality work.

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: [email protected]
• Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.