R&D Staff Engineer

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

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.

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Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Are you passionate about improving and expanding the possibilities of Cardiovascular Ready to join a team thats reimagining how we heal Our Cardiovascular team develops leading solutions for heart recovery electrophysiology and stroke. You will join a proud heritage of continually elevating standards of care for stroke heart failure and atrial fibrillation (AFib) patients.

Your unique talents will help patients on their journey to wellness. Learn more at are searching for the best talent for a R&D Staff Engineer to support our Electrophysiology business. This role will work fully on-site in our Irvine CA office.

Primary Function of Position

The Staff R&D Engineer is responsible for the technical development of therapeutic systems at J&J Medtech Electrophysiology. Their focus will be on the mechanical/electrical design of advanced energy catheters and accessories contributing to the advancement of both our therapeutic and diagnostic systems. They will be a responsible member of the R&D team supporting innovative technology development and commercialization. They will have both the technical depth to resolve complex mechanical material and manufacturing design issues as well as the ability to work in an interdisciplinary team to troubleshoot and root cause higher level system issues. They must have strong technical depth in relevant areas and have a track record of successful product development efforts. Using their subject matter expertise exceptional communication skills and cross-functional collaboration they will investigate and develop catheters and/or accessories that are part of our therapeutic and diagnostic EP ecosystem. They must excel in a high-energy focused small-team environment and have a commitment to high quality prototypes and concepts. A strong sense of shared responsibility and shared reward is required as well as a commitment to high product quality.

Essential Job Duties

• Work in a small cross-functional project team to design develop and verify new catheters/cables.
• Develop implement test and document new solutions processes and designs according to corporate standards and departmental operating procedures
• Hands-on assembly and testing of devices to support proof of concept design development pre-clinical and V&V activities
• Investigate and determine root cause of emerging design or manufacturing defects/failures.
• Develop product concepts and assess with physicians and healthcare staff identifying feature set use conditions design requirements/specifications and completing tradeoff analysis.
• Development and documentation of design and manufacturing documentation including inspection procedures assembly instructions test methods purchase specifications BOMs part and assembly drawings using appropriate change control procedures
• Establish individual goals consistent with overall project goals
• Performs other duties as required to support the companys overall strategy and goals

Required Skills and Experience:

• A minimum of 6-8 years of relevant experience with a Bachelors degree minimum of 4-6 years with a masters
• Demonstrated ability to work in cross-functional research and development teams
• Experience with FDA QSR 21 CFR Part 820 ISO 13485 and other related standards
• Demonstrated ability to originate novel concepts and rapidly convert ideas into functional prototypes to evaluate technical feasibility and clinical value
• Proven track record operating in highly ambiguous environments with limited data effectively identifying key risks and prioritizing experiments to accelerate learning
• Strong capability to define early product architecture and translate feasibility prototypes into scalable design-controlled development programs
• Demonstrated ability to determine what to prototype versus what to analyze balancing speed risk reduction and long-term scalability
• Expertise in structured problem-solving and rapid design iteration cycles (buildtestlearn)
• Hands-on experience with rapid prototyping methods including 3D printing plastics processing metal fabrication and bench-level assembly
• Proficiency in CAD-based mechanical design (SolidWorks preferred)
• Experience with all phases of the product development lifecycle; including proof-of-concept design implementation debug verification qualification and transfer
• High autonomy and ability to work independently under limited supervision to determine and develop approach to solutions.
• Ability to communicate effectively (written oral) across all levels and organizations

Required Education and Training:

• Minimum education: BS or MS in Mechanical Engineering or related engineering or scientific discipline or equivalent work experience

Preferred Skills and Experience:

• Experience with energy delivery devices is a strong plus

Johnson & Johnson is an 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 disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via Internal employees contact AskGS to be directed to your accommodation resource.

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Staff IC