Quality Engineer I

J&J FAMILY OF COMPANIES

Warsaw, Indiana, United States of America
Onsite
Quality management system adherence
Fda 21 cfr 820 compliance
Iso 13485 regulatory requirements
Johnson & Johnson is committed to building innovative healthcare solutions that prevent, treat, and cure complex diseases while delivering smarter and less invasive treatments

Job Summary

  • Johnson & Johnson is committed to building innovative healthcare solutions that prevent, treat, and cure complex diseases while delivering smarter and less invasive treatments.
  • The Quality Engineer I role supports new product introduction, continuous improvement initiatives, and quality compliance with a focus on manufacturing operations under general supervision.
  • The position is located in Warsaw, Indiana, and may require up to 10% domestic or international travel, with a commitment to diversity and inclusion in the workplace.

Matching Summary

Johnson & Johnson is committed to building innovative healthcare solutions that prevent, treat, and cure complex diseases while delivering smarter and less invasive treatments.

Skills & Requirements

Must-have

  • Quality Management System adherence
  • FDA 21 CFR 820 compliance
  • ISO 13485 regulatory requirements
  • GMP and ISO regulated industry experience
  • Quality issue investigation and resolution
  • Support for validation activities

Nice-to-have

  • Introductory knowledge of manufacturing equipment
  • Statistical techniques and software knowledge
  • Project management skills
  • Strong verbal communication
  • Technical writing ability
  • Hands-on problem solving
  • Attention to detail

Key Requirements

  • Bachelor's Degree in Engineering or equivalent
  • 0 – 2 years experience in FDA regulated environment
  • Experience in GMP and/or ISO regulated industry
  • Proficient English communication
  • Ability to travel up to 10%

Work Rights

Not specified

Tailored Resume

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