Regulatory Affairs Specialist - Fully Remote

Mercor
New York, NY
Remote
Job Description
Regulatory Affairs Specialist - Fully Remote. Medical Devices Expert. Build a realistic digital workspace, design multi-step tasks, and collaborate with medical-device experts.

Requirements

  • 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.
]]>