SR. QUALITY ENGINEER, NPD

Johnson & Johnson is currently recruiting for a Senior Quality Engineer, NPD to be based in Irvine, CA.
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 https://www.
nj.
om/.
The Senior Quality Engineer – plans, coordinates and executes quality assurance activities intended to ensure effective product quality processes are in place and executed throughout lifecycle of product.
Involved in New Product Development (NPD) teams and other activities to develop products, design verification tests, process validations and quality processes to ensure compliance with the company’s Quality System policies and procedures and applicable external requirements and standards.
As needed, assists to develop quality-engineered systems and products, and support qualification and validation activities.
Will be considered a subject matter expert (SME) on Quality matters, relevant Quality tools and will work on complex problems and projects.
Will show leadership in driving program/projects and innovating compliant approaches and solutions to problems.
Shares technical expertise with others and develop other engineers.
A few of the responsibilities may involve collaborating with other members of the Design Team.
Will contribute to activities including risk management document development, creation, and design of catheter test methods, authoring of test protocols, and testing of products during their development cycle.
Duties include.
• Working with other functional groups, including R&D and Operations in support of new product development, engineering projects, quality assurance activities, and lifecycle management.
• Utilizing Quality Engineering tools/processes in development and implementation of practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecycle.
• Oversight, from a Quality NPD perspective, of the Non-Conformance Report (NCR) process for BWI facilities located in the U.
.
• Develop and establish effective quality control and support associated risk management plans, AFMEA, DFMEA and PFMEA.
• Write, review and/or approve process and product validation protocols and reports, equipment qualifications, engineering change orders.
• Use statistical tools to analyze data, make acceptance decisions, and improve process capability (Six Sigma, Statistical Process Control (SPC), Design of Experiments (DOE), etc.).
Performs statistical analysis of data generated including but not limited to.
Gauge R&R, ANOVA, Sample Size determination and variable/attribute data analysis against predetermined acceptance criteria.
• Ensure that development activities follow design control requirements (Design Trace Matrix), product is tested per applicable standards, GSPR are met per the MDR, and product is properly transferred to manufacturing per applicable specifications.
• Technical problem solving, failure analysis, and root cause determination.
• Makes decisions independently on engineering problems and methods and represents the organization in conferences to resolve important questions and to plan and coordinate work.
• Recommend issue resolution to management for significant capability and compliance issues.
• Works closely with functional leadership in planning and executing project milestones.
• Plans, develops, coordinates, and directs one or more large important engineering projects or several small projects with many complex features.
• Carries out complex or novel assignments requiring the development of new or improved techniques or procedures.
• Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment, when necessary, data are insufficient or confirmation by testing is advisable.
• Responsible for communicating business related issues or opportunities to next management levels.
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures • Performs other duties assigned as needed Qualifications Education.
• Bachelor’s degree, required; preferably in engineering and/or equivalent scientific discipline Required Experience & Skills.
• A minimum of 4 years of quality, manufacturing, or research and development experience in a medical device or other regulated industry • Ability to define problems, collect and analyze data, establish facts, and draw conclusions and recommendations • Ability to use broad knowledge of regulatory, technical, and business requirements to conduct due diligence assessments • Ability to apply project management skills to ensure fulfillment of new product development requirements • Ability to develop and implement Quality standards • Demonstrated auditing and problem-solving skills • Knowledge of leading-edge Quality Engineering, design control, and verification and validation (V&V) tools and methodologies • Ability to effectively collaborate and communicate with internal and external partners at all levels of the organization including influencing and negotiating resulting in positive business and quality outcomes.
Preferred Experience & Skills.
• Six Sigma/ Design for Six Sigma experience, and/or knowledge of Process Excellence tools • Lean manufacturing experience • Understanding of theoretical and practical fundamentals and experimental engineering techniques such as DOE, DMAIC and ANOVA.
• Knowledge of Quality and operations systems and processes, including GMP • Working knowledge of SolidWorks, other CAD based programs (ie.
basic dimensioning, tolerance stack analysis) is a plus.
• Experience with Minitab, R and other statistical software is a plus.
• Geometrical Dimensioning and Tolerancing (GD&T) experience with an understanding of ASME Y14.
Y.
Other.
• This position is located in Irvine, California and will require up to 20% travel domestic and international.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
The anticipated base pay range for this position is to The Company maintains highly competitive, performance-based compensation programs.
Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan.
The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year.
Bonuses are awarded at the Company’s discretion on an individual basis.