Johnson & Johnson

R&D Staff Engineer

Johnson & Johnson$109K — $174K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 6-8 years of experience with a Bachelor's degree; 4-6 years with a Master's degree.
  • Cross-functional R&D team experience.
  • Knowledge of FDA QSR 21 CFR Part 820 and ISO 13485 standards.
  • Proven ability to develop novel concepts into functional prototypes.
  • Experience managing product architecture and design-controlled development programs.

Responsibilities

  • Design, develop, and verify new catheters and cables in a small team setting.
  • Implement and document new solutions and designs according to corporate standards.
  • Perform hands-on assembly and testing for device proof of concept and design development.
  • Identify root causes of design and manufacturing defects or failures.
  • Collaborate with healthcare professionals to develop product concepts and specifications.

Benefits

  • Vacation - 120 hours per year.
  • Sick time - 40 to 56 hours per year, depending on state.
  • Holiday pay - 13 days per year.
  • Parental Leave - 480 hours within one year of a child’s birth/adoption.
  • Volunteer Leave - 32 hours per year.
Full Job Description
Job Function:
R&D Product Development

Job Sub Function:
R&D Mechanical Engineering

Job Category:
Scientific/Technology

All Job Posting Locations:
Irvine, California, United States of America

Job Description:

Fueled by innovation at the intersection of biology and technology, we're 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 that's 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 https://www.jnj.com/medtech

We 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 company's 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 (build-test-learn)
  • 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


Required Skills:

Preferred Skills:
Business Case Modeling, Coaching, Critical Thinking, Design Thinking, Feasibility Studies, Mechanical Engineering, Problem Solving, Process Oriented, Product Design, Product Development, Project Management Methodology (PMM), Project Support, Research and Development, SAP Product Lifecycle Management, Technical Credibility, Technical Writing, Technologically Savvy

The anticipated base pay range for this position is :
$109,000.00 - $174,800.00

Additional Description for Pay Transparency:
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

Vacation -120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year

Holiday pay, including Floating Holidays -13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave - 80 hours in a 52-week rolling period10 days

Volunteer Leave - 32 hours per calendar year

Military Spouse Time-Off - 80 hours per calendar year

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

Johnson & Johnson Careers

Joining Johnson & Johnson provides an unparalleled opportunity to be a part of a global team of professionals dedicated to blending care, science, and innovation to profoundly change the trajectory of health for humanity.

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At Johnson & Johnson, you will engage in work that matters. Join our community of professionals in health care to drive significant and impactful changes across the globe. Our team at Johnson & Johnson leads with science and heart in sectors from pharmaceuticals to medical devices and consumer health products.

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Engage in groundbreaking work that enhances how care is delivered on a global scale. Johnson & Johnson’s commitment to innovative health solutions results in dynamic career paths filled with opportunities for professional growth and development.

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Our team at Johnson & Johnson thrives on collaboration and diversity. You will work alongside over 130,000 employees globally who are committed to making a lasting impact. With a culture that values diversity training and leadership, you are supported in both personal and professional growth.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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