Engineer 2 Development Engineering

Biosense Webster Inc., a Johnson & Johnson Company, is currently recruiting for an Engineer 2 Development Engineering to support the development of components for its Catheter New Product Development group, located in Irvine, CA. Atrial fibrillation (AFIB) is a quivering or irregular heartbeat (arrhythmia) that can lead to blood clots, stroke, heart failure and other heart-related complications. 20 million people around the world suffer from AFIB each year. Biosense Webster, Inc. is the global leader in the science of diagnosing and treating heart rhythm disorders. The company established its leadership in electrophysiology with the development of the first real-time, 3D cardiac mapping and navigation technology, as well as the first electrophysiology catheter. The introduction of the company’s CARTO® 3 System in 2009 revolutionized 3D mapping technology by increasing the accuracy, speed, and efficiency of the cardiac ablation procedure. Our engineers and technologists are on the forefront of technology in the medical device industry. You will be making a significant contribution to the New Product Development (NPD) pipeline and redefining patient care through innovation. Our Development Engineers are a critical resource within NPD teams, developing robust component designs and manufacturing processes that meet or exceed all product requirements at the lowest possible manufacturing cost. This is an exciting opportunity to deliver innovation in the growing Catheter franchise. Under limited supervision, performs and documents moderately complex technical functions relating to component design, development, qualification and induction in to production. Performs electrical, mechanical, electromechanical, developmental Design duties in New Product Development engineering. KEY RESPONSIBILITIES: Under (e.g. limited supervision, general direction, etc.) and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: Execute design, development, qualification and stabilization of component (metal, plastic, electrical or other) and process solutions Own process development, qualification, and control for component and assembly solutions Serve as an integral part of NPD teams on Design for Manufacturing/Assembly/ Cost and drive robust product and process development that meets business commitments and stabilization metrics Design and develop robust equipment, tooling, and manufacturing processes to meet product requirements in compliance with User requirements, Quality, Regulatory, Safety and Ergonomic standards Incorporate risk mitigation methodology to drive process stability and capability Identify and implement standard methodologies of project management through component development Responsible for developing new manufacturing and assembly processes consistent with Design for Manufacturability for new product introductions Responsible for communicating business related issues or opportunities to next management level Responsible for ensuring personnel and Company compliance with all Federal, State, local and Company regulations, policies, and procedures Performs other duties assigned as needed Qualifications Minimum of a bachelor’s degree, preferably in Engineering, combined with at least 3 years work-related engineering experience is required. Prior experience in New Product Development, working in a team environment is required. Experience working closely with external suppliers is required. Ability to read, interpret, redline, and make recommendations on engineering drawings is preferred. Previous experience in the areas of Design for Manufacturing or Assembly is preferred. Experience with Measurement Systems Analysis (i.e. GR&R) is preferred. Statistical Analysis knowledge (i.e. Design of Experiments, Process Stability/Control/Capability) is preferred. Knowledge of good manufacturing practices and documentation, preferably in the medical industry is preferred. Knowledge of various manufacturing processes to make metal, plastic and/or electrical components is preferred. Experience within a medical device production environment or other regulated environment is preferred. Tolerance stackup, GD&T experience is preferred. Six Sigma Green belt certification is preferred. This position may require up to 25% domestic travel and up to 10% International travel. At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional, and financial health of our employees and the ones they love. As such, candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com. Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law Primary Location United States-California-Irvine-31 Technology Dr Organization Biosense Webster Inc. (6010) Job Function Engineering Requisition ID 2206020215W