Quality Engineer
Johnson & Johnson · Jacksonville, FL
QualityFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Quality Engineer position at Johnson & Johnson's MedTech manufacturing facility in Jacksonville, Florida. The role involves managing quality events and nonconformances, conducting investigations, and applying engineering tools to sustain product and process standards in a regulated medical device environment.
What they're looking for
- Bachelor's degree in Engineering or related technical field
- 0-2 years of related quality or manufacturing experience
- Knowledge of product/process risk management and FDA/ISO standards
- Ability to perform hands-on troubleshooting and problem-solving
- Understanding of GMP/ISO regulations and manufacturing equipment
- Willingness to work C shift (6am-6pm)
What you'll be doing
- Review device history records for quality standards and document nonconformances
- Conduct and approve investigations to determine root causes and reduce recurrence
- Support material segregation and defect classification efforts
- Execute quality tools and develop metrics for manufacturing processes and customer feedback
- Ensure compliance with SOPs and regulatory requirements including FDA and ISO standards
Privacy & handoff
This role links to Johnson & Johnson's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.