Regulatory Affairs Expert - Fully Remote | Upto $1450 Part-time

Mercor
New York, NY
Job Description
Regulatory Affairs Expert needed for a contract role. Must have 3+ years of experience in regulatory affairs, quality engineering, R&D, manufacturing engineering, or clinical affairs. Competitive task completion pay and performance bonus.

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
  • Certifications: RAC, ASQ CQE/CRE/CBA (optional)

Benefits

  • Competitive task completion pay
  • Performance bonus
  • Hourly opportunity for sustained quality and throughput
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