Associate Quality Engineer

Globus Medical

Methuen, MA, United States
**
Bachelor's degree in science or engineering
Knowledge of gmp and iso 13485
Root cause analysis and corrective actions
** Globus Medical is seeking an Associate Quality Engineer to enhance manufacturing quality and ensure compliance with medical device regulations. The ideal candidate will have a background in quality assurance, preferably in the medical device industry, and strong problem-solving skills. **

Job Summary

  • The Associate Quality Engineer will ensure compliance with US FDA and international medical device regulations while maintaining the highest quality standards.
  • This role involves leading nonconforming material reviews, facilitating Material Review Board activities, and driving continuous improvement in quality workflows.
  • Candidates must possess strong communication skills and the ability to collaborate with cross-functional teams including Product Development, Operations, and Regulatory affairs.

Matching Summary

Match Score: 75

** Globus Medical is seeking an Associate Quality Engineer to enhance manufacturing quality and ensure compliance with medical device regulations. The ideal candidate will have a background in quality assurance, preferably in the medical device industry, and strong problem-solving skills. **

Skills & Requirements

Must-have

  • Bachelor's degree in science or engineering
  • Knowledge of GMP and ISO 13485
  • Root cause analysis and corrective actions
  • Experience with FDA and international regulations
  • Proficiency in MS Office and statistical tools

Nice-to-have

  • Lean Manufacturing and Six Sigma knowledge
  • Reliability engineering experience
  • Strong critical thinking and problem-solving skills
  • Ability to work in a deadline-driven environment
  • Team player capable of cross-functional collaboration

Key Requirements

  • Bachelor's Degree required (science or engineering preferred)
  • 0-2 years' experience in quality assurance
  • Medical device industry experience preferred
  • GMP and ISO experience required

Work Rights

Not specified

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