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.

Learn more at

Job Function:

R&D Product Development

Job Sub Function:

Biomedical Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Cincinnati, Ohio, United States of America

Johnson & Johnson is currently recruiting for a Staff Quality Engineer! This position will be located in Cincinnati, Ohio.

• This position will support New Product Development or Lifecycle Engineering within the Energy Quality organization, based in Cincinnati, OH
• This position will support the Energy franchise that may include Harmonic, Advanced Bipolar, Capital and Megadyne.
• Defines, leads and implements state-of-the-art quality engineering focus and improvements in design and development of products, and in transfer and steady state phases of manufacturing operations.
• Influences the company's business, tactical directions, and financial results through a sharing of technical expertise. Performs complex design analysis and provides input or approval for detailed design specifications, tooling, fabrication, and testing.
• At this level the role has increased responsibility including, but not limited to, additional skills, multiple lines/products, diverse teams, etc.

• Supports the continuous improvement of quality systems to facilitate business and quality objectives, and compliance review and resolution processes.
• Alerts the organization to issues in time to resolve potential adverse effects on the customer, company image, or reputation of the business.
• Oversees the quality engineering group to implement engineering and quality systems, and regulatory compliance strategies and objectives.
• Conducts basic technical design reviews and facilitates the implementation and utilization of quality tools within research and development and new product development.
• Researches and compiles worldwide regulatory and technical standards for shift in design related quality trends.
• Directs the work assignments of engineers to support effective quality engineering processes at all levels and throughout the engineering organization.
• Oversees engineers in development and deployment of innovative quality engineering tools, techniques and systems.
• Oversees the implementation of world with focus on business results including prevention and detection of defects at earliest phase of product design, continuous improvement and customer satisfaction.
• Provides support to Johnson and Johnson process excellence initiatives including six sigma, design excellence, and lean thinking.
• Oversees engineering operations, scientific evaluations of new products, technology concepts and development.
• Purchases or designs equipment that meets health, safety and environmental standards set by the company.
• Performs design reviews and pre-validation assessments to ensure the safe and environmentally sound startup of new processes.
• Assures compliance with all local government and company regulations, policies and procedures.
• Provides statistical support for design of experiments, sampling plans, capability assessments, and hypothesis tests.
• Researches and reports on competitors' design strengths and weaknesses.
• Provides technical expertise across a broad range of engineering areas and methodologies.
• Leads and oversees the activities of engineers and support staff.
• Responsible for communicating business related issues or opportunities to next management level.
• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
• Performs other duties assigned as needed.
• May support technical training (i.e. statistics and quality methods) and teaching/mentoring of other

• A minimum of 6 years of work experience in a regulated industry (medical device, biopharmaceutical, or pharmaceutical) or veterans with leadership experience
• Advanced knowledge of Quality Engineering/Scientific methods and techniques
• Applied statistics of growing complexity
• Test method development, statistics, and reliability
• Experience working within a team, acquiring feedback, negotiating, and training
• Understand new concepts quickly, research and maintain ongoing learning of industry regulations
• Fundamental technical understanding of…