Johnson & Johnson
Senior Engineer, R&D
Johnson & Johnson, Irvine, California, United States, 92713
Job Description - Senior Engineer, R&D (2406217608W)DescriptionJ&J MedTech is recruiting for a
Senior Engineer, R&D
located in
Irvine, CA.J&J MedTech is the global leader in the science of diagnosing and treating heart rhythm disorders. J&J MedTech 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.Patients with atrial fibrillation (Afib) can be at high risk for developing clot formation in the left atrial appendage (LAA) which can lead to strokes and other complications. The LAA is a small pouch in the left atrium of the heart that is a major contributor to thromboembolic stroke in patients with atrial fibrillation. In order to mitigate the stroke risk, patients with AFib undergo a surgical procedure to close the left atrial appendage (LAA) in patients with non-valvular atrial fibrillation.J&J MedTech is currently recruiting for a Senior Engineer, R&D to support catheter and sheath engineering projects related to the development of its new LAA closure system. The Senior Engineer will be supporting a dynamic, fast-paced, close-knit team to fully develop new products. Project support includes design and documentation of effective and efficient tools, fixtures, and machines for the manufacture of Company products and assists in the design, fabrication, and testing of company products in the feasibility stage. A passion for hands-on problem solving and prototyping is a must.Key Responsibilities:Support the design of new/existing components while ensuring all design requirements are met.Develop and execute test methods, procedures, work instructions, and reports with little supervision.Implement complex design concepts and ideas into working drawings, solid models, and prototypes.Study specifications, engineering blueprints, tool orders, and shop data and confer with engineering and shop personnel to resolve design problems related to material characteristics, dimensional tolerances, service requirements, manufacturing procedures, and cost.Develop concepts, designs, and details for machines, tools, and fixtures.Assist with the inspection of components and fixtures after fabrication to ensure that they meet end specifications.Interface between external vendors and internal core team members.Prototype design and perform feasibility assessments at a rapid pace.Conduct complex or novel assignments requiring the development of new or improved techniques or procedures.Work hands-on to both manufacture and evaluate the feasibility of prototypes.Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.Qualifications:Required:A minimum B.S (Mechanical, Biomedical Engineering, or equivalent) with industry experience.Experience with CAD software (Solidworks, Creo or similar) is required.Collaborative teammate with strong communication skills, written and verbal required.Ability to come up with creative solutions to solve technical issues.A general understanding of concept development, 3D modeling, creating 2D drawings (good understanding of GD&T, and manufacturing methods), and rapid prototyping.Ability to work with outside vendors for procuring parts.Travel up to 20% may be required.Preferred:M.S. (Mechanical, Biomedical Engineering, or equivalent) or higher education.Able to write and communicate clearly, including generating and presenting well-written reports is preferred.General understanding of test method development, setup, and execution along with equipment setup and validation is preferred.Prior experience with inspection of components is preferred.Medical Device experience with 4+ years of experience.Structural heart experience highly preferred.Experience with nitinol related devices.Knowledge and experience in product development processes.Experience with statistical analysis.
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Senior Engineer, R&D
located in
Irvine, CA.J&J MedTech is the global leader in the science of diagnosing and treating heart rhythm disorders. J&J MedTech 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.Patients with atrial fibrillation (Afib) can be at high risk for developing clot formation in the left atrial appendage (LAA) which can lead to strokes and other complications. The LAA is a small pouch in the left atrium of the heart that is a major contributor to thromboembolic stroke in patients with atrial fibrillation. In order to mitigate the stroke risk, patients with AFib undergo a surgical procedure to close the left atrial appendage (LAA) in patients with non-valvular atrial fibrillation.J&J MedTech is currently recruiting for a Senior Engineer, R&D to support catheter and sheath engineering projects related to the development of its new LAA closure system. The Senior Engineer will be supporting a dynamic, fast-paced, close-knit team to fully develop new products. Project support includes design and documentation of effective and efficient tools, fixtures, and machines for the manufacture of Company products and assists in the design, fabrication, and testing of company products in the feasibility stage. A passion for hands-on problem solving and prototyping is a must.Key Responsibilities:Support the design of new/existing components while ensuring all design requirements are met.Develop and execute test methods, procedures, work instructions, and reports with little supervision.Implement complex design concepts and ideas into working drawings, solid models, and prototypes.Study specifications, engineering blueprints, tool orders, and shop data and confer with engineering and shop personnel to resolve design problems related to material characteristics, dimensional tolerances, service requirements, manufacturing procedures, and cost.Develop concepts, designs, and details for machines, tools, and fixtures.Assist with the inspection of components and fixtures after fabrication to ensure that they meet end specifications.Interface between external vendors and internal core team members.Prototype design and perform feasibility assessments at a rapid pace.Conduct complex or novel assignments requiring the development of new or improved techniques or procedures.Work hands-on to both manufacture and evaluate the feasibility of prototypes.Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.Qualifications:Required:A minimum B.S (Mechanical, Biomedical Engineering, or equivalent) with industry experience.Experience with CAD software (Solidworks, Creo or similar) is required.Collaborative teammate with strong communication skills, written and verbal required.Ability to come up with creative solutions to solve technical issues.A general understanding of concept development, 3D modeling, creating 2D drawings (good understanding of GD&T, and manufacturing methods), and rapid prototyping.Ability to work with outside vendors for procuring parts.Travel up to 20% may be required.Preferred:M.S. (Mechanical, Biomedical Engineering, or equivalent) or higher education.Able to write and communicate clearly, including generating and presenting well-written reports is preferred.General understanding of test method development, setup, and execution along with equipment setup and validation is preferred.Prior experience with inspection of components is preferred.Medical Device experience with 4+ years of experience.Structural heart experience highly preferred.Experience with nitinol related devices.Knowledge and experience in product development processes.Experience with statistical analysis.
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