Quality Engineer

Globus Medical

Memphis, TN, United States
Fda and iso 13485 compliance
Design verification and validation
Non-conforming material program support
The role involves designing and maintaining quality assurance protocols for processing materials into finished medical products

Job Summary

  • The role involves designing and maintaining quality assurance protocols for processing materials into finished medical products.
  • Candidates must ensure compliance with FDA regulations, ISO 13485 standards, and international safety requirements.
  • The position supports risk assessment, design control activities, and sterilization validation to improve patient outcomes.

Matching Summary

The role involves designing and maintaining quality assurance protocols for processing materials into finished medical products.

Skills & Requirements

Must-have

  • FDA and ISO 13485 compliance
  • Design verification and validation
  • Non-conforming material program support
  • Incoming materials inspection
  • Process change qualification

Nice-to-have

  • Strong analytical and problem-solving skills
  • Teamwork and collaboration abilities
  • Attention to detail and organization
  • MS Office proficiency
  • Ethical business practices adherence

Key Requirements

  • Bachelor's degree in engineering discipline
  • Minimum 2 years of related experience
  • Knowledge of FDA and state regulations
  • Experience with ISO 13485 standards

Work Rights

Not specified

Tailored Resume

Cover Letter