Quality Engineer

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

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As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Supply Chain Engineering

Quality Engineering

Scientific/Technology

Jacksonville, Florida, United States of America

We are searching for the best talent for a Quality Engineer to be based in Jacksonville, FL.

Fueled by innovation at the intersection of biology and technology, we are developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at

The Quality Assurance Engineer assists with quality events, nonconformances, and associated tasks at our Jacksonville Manufacturing site. They utilize Quality Engineering tools and practices to effectively and efficiently manage nonconformances and ensure key metrics are met. They coordinate phases of work internally and externally. They apply Quality Engineering principles and problem-solving skills to enhance and sustain products and processes aligned with overall quality and business vision.

Harsh environments and ambiguous problems are managed to prevent unanticipated failure modes and improve process capability. This person will support processes in base business.

• Responsible for review of electronic and/or manual device history records for quality standards and utilizes non-conformance for document issues as needed.
• Conducts investigations, develops investigations, reviews and approves investigations, and initiates projects designed to reduce recurrence.
• Supports investigations for root cause determinations, material segregation, classification of defect types including application of new techniques or study designs.
• Ensures compliance to SOPs and regulatory requirements including FDA and ISO regulations.
• Executes quality tools and develops quality metrics for manufacturing processes and customer feedback.
• Acts as a change agent to improve compliance and quality culture.

• Bachelors or equivalent degree, preferably in Engineering or a related technical field.

• 0-2 years of related experience.
• Knowledge of product/process Risk Management (FDA and ISO standards).

• Experience working in a regulated environment is helpful.
• Experience working in a manufacturing environment is helpful.
• Ability to perform hands-on troubleshooting and problem solving is preferred. The ability to think on the feet and providing sound judgment is highly desired.
• The ability to perform hands-on troubleshooting and problem solving is helpful.
• Good technical understanding of manufacturing equipment and processes is helpful.
• A thorough understanding of GMP/ISO regulations is helpful.

• Shift position – C shift 6a-6pm

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual…