Quality Engineer I

Johnson & Johnson MedTech Orthopedics

Warsaw, Indiana, United States of America
Onsite
Quality management system adherence
Fda 21 cfr 820 compliance
Iso 13485 compliance
Apply basic Quality Engineering/Scientific Method techniques and principles to daily tasks and activities under general supervision

Job Summary

  • Apply basic Quality Engineering/Scientific Method techniques and principles to daily tasks and activities under general supervision.
  • Support resolution of Quality Issues, including investigation, bounding, actions, reviews, and approval of non-conformances, CAPAs, and audit findings.
  • This role supports new product introduction, continuous improvement initiatives, and base business products and processes (risk management, nonconformances, inspection methods, etc.).

Matching Summary

Apply basic Quality Engineering/Scientific Method techniques and principles to daily tasks and activities under general supervision.

Skills & Requirements

Must-have

  • Quality Management System adherence
  • FDA 21 CFR 820 compliance
  • ISO 13485 compliance
  • GxP compliance
  • non-conformance investigation
  • CAPA support

Nice-to-have

  • critical thinking
  • attention to detail
  • hands-on problem solving
  • statistical techniques understanding
  • project management skills

Key Requirements

  • Bachelor's Degree in Engineering
  • 0-2 years GMP/ISO regulated industry experience
  • Introductory Quality Engineering knowledge
  • English verbal and written communication

Work Rights

Not specified

Tailored Resume

Cover Letter