Complaints Specialist I, Temporary

Terumo Medical Corporation

Elkton, MD, US
On-site
Fda and iso regulatory compliance
Medical device complaint handling
Root cause analysis
The Complaint Handling Specialist I is responsible for analyzing and controlling customer complaints in compliance with FDA, ISO, QSR, and other regulatory guidelines

Job Summary

  • The Complaint Handling Specialist I is responsible for analyzing and controlling customer complaints in compliance with FDA, ISO, QSR, and other regulatory guidelines.
  • Key responsibilities include investigating customer complaints, testing returned samples, assisting with MDR and Vigilance reports, and collaborating with cross-functional teams.
  • Terumo offers competitive benefits including annual bonus, paid time off, health benefits, 401(k) with matching, and tuition reimbursement.

Matching Summary

The Complaint Handling Specialist I is responsible for analyzing and controlling customer complaints in compliance with FDA, ISO, QSR, and other regulatory guidelines.

Skills & Requirements

Must-have

  • FDA and ISO regulatory compliance
  • Medical device complaint handling
  • Root cause analysis
  • Customer interaction
  • Device History Record review

Nice-to-have

  • Collaborative team environment
  • Personal growth opportunities
  • Innovation and problem-solving
  • Advancing healthcare with heart

Key Requirements

  • Minimum 2 years experience in quality or customer service/complaint resolution in medical device industry
  • High school diploma required; Associate's Degree preferred
  • Must have US work authorization

Work Rights

Must have US work authorization

Tailored Resume

Cover Letter