Quality Engineer - MedTech Manufacturing, Jacksonville

Johnson & Johnson MedTech; Jacksonville (FL); On-site; USD 65,000 - 90,000; Full time

Job summary

Johnson & Johnson MedTech is seeking a Quality Engineer for the Jacksonville, FL site. The role focuses on quality events, nonconformances, and applyingQuality Engineering tools to improve products and processes.

The engineer will support manufacturing and regulatory compliance, including FDA/ISO guidelines. Responsibilities include reviewing device history records, investigating issues, and driving corrective actions.

Qualifications

• Bachelor's degree in Engineering or related technical field.
• 0-2 years of related experience.
• Knowledge of product/process risk management (FDA and ISO standards).
• Experience working in a regulated/manufacturing environment is helpful.
• GMP/ISO regulations familiarity is beneficial.

Responsibilities

• Review device history records for quality standards and manage non-conformances.
• Conduct and support investigations to determine root causes and implement corrective actions.
• Support root cause determinations, material segregation, defect classification; apply new study designs.
• Ensure compliance with SOPs and regulatory requirements (FDA/ISO).
• Develop quality metrics and support continuous improvement in manufacturing processes.

Skills

Quality Assurance

Root Cause

GMP/ISO

Problem Solving

Risk Management

Education

Bachelor's degree in Engineering

Job description

Johnson & Johnson MedTech is seeking a Quality Engineer for the Jacksonville, FL site. The role focuses on quality events, nonconformances, and applyingQuality Engineering tools to improve products and processes.

The engineer will support manufacturing and regulatory compliance, including FDA/ISO guidelines. Responsibilities include reviewing device history records, investigating issues, and driving corrective actions.