Service 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 MedTech, 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. Learn more at jnj.com 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. Job Function: Supply Chain Engineering Job Sub Function: Quality Engineering Job Category: Scientific/Technology All Job Posting Locations: Cincinnati, Ohio, United States of America Job Description:

Johnson & Johnson MedTech is recruiting for a Service Quality Engineer, located in Cincinnati, OH. At Johnson & Johnson, we believe health is everything. The Service Quality Engineer plays a key role in supporting the quality and compliance of service and repair operations for J&J MedTech Surgery Energy products. This position partners closely with Service Engineering, Complaint Management, Service Solutions, and cross-functional teams to ensure service processes meet quality, regulatory, and customer requirements while driving continuous improvement initiatives. Key Responsibilities : In accordance with all applicable federal, state, and local laws/regulations and Johnson & Johnson policies and procedures, this position is responsible for: Provide quality engineering support for service and repair operations in the Cincinnati Service Center and international service centers. Support complaint investigations, nonconformance management, CAPAs, and audit readiness activities. Analyze quality metrics and trends to identify opportunities for process improvements and risk reduction. Collaborate with new product introduction and lifecycle management teams to ensure serviceability and repair considerations are incorporated into product development. Support quality and cost improvement projects that enhance service performance and customer satisfaction. Partner with cross-functional teams to maintain compliance with quality systems, regulatory requirements, and company policies. Assist in evaluating repaired products, spare parts, and service processes to improve efficiency and effectiveness.

Education: A bachelor’s degree in a Science, Engineering, Technology, or Mathematics (STEM) field is strongly preferred. Non-STEM graduates with additional technical training or experience will also be considered. Experience and Skills: Required: Minimum of 2 years of professional experience. Strong analytical, problem-solving, and communication skills. Proficiency with Microsoft Office applications, including Excel, PowerPoint, and Word. Ability to work effectively in a cross-functional and collaborative environment. Preferred: Experience in a regulated medical device, pharmaceutical, or biopharmaceutical environment. Knowledge of quality systems, CAPA, root cause analysis, risk management, validation, and process improvement methodologies. Familiarity with Lean, Six Sigma, DMAIC, DMADV, FMEA, MSA, statistical process control, or related quality engineering tools. Travel: Up to 10% Required Skills:

Customer Centricity, Data Savvy, Document Management, Execution Focus, Good Automated Manufacturing Practice (GAMP), Issue Escalation, Lean Supply Chain Management, Process Control, Process Improvements, Quality Control Testing, Quality Services, Quality Standards, Quality Systems Documentation, Science, Technology, Engineering, and Math (STEM) Application, Supervision,