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Johnson & Johnson

Staff R&D Engineer

Reposted 3 Days Ago
Be an Early Applicant
In-Office
Irvine, CA, USA
109K-175K Annually
Mid level
In-Office
Irvine, CA, USA
109K-175K Annually
Mid level
The Staff R&D Engineer will provide mechanical engineering support throughout product design, development, and commercialization, ensuring compliance and quality in the product lifecycle.
The summary above was generated by AI

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 jnj.com

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.

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:

Johnson & Johnson MedTech, a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Staff R&D Engineer, located in Irvine, CA.

About MedTech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, and more personalized treatments. Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech

Overview

The Staff R&D Mechanical Engineer is a seasoned individual contributor responsible for delivering engineering expertise across all stages of the product lifecycle. This role applies advanced engineering principles to support device design, development, verification, validation, and manufacturing transfer of regulated medical devices, with a strong focus on catheter-based technologies. The role partners closely with cross‑functional teams to deliver safe, effective, and compliant products to market.

Key Responsibilities

  • Provide advanced mechanical engineering support throughout design, development, verification, validation, and commercialization of medical devices.

  • Lead and contribute to device design and development activities, including component and system-level design.

  • Support and review Design Verification Testing (DVT) and Verification & Validation (V&V) activities to ensure compliance with regulatory and product requirements.

  • Apply proven scientific and engineering methodologies to develop high-quality, innovative products.

  • Collaborate closely with Manufacturing, Quality, Regulatory, and Clinical partners to support design for manufacturability and smooth product transfer.

  • Investigate, document, and resolve reported incidents to maintain product quality and reliability.

  • Prepare and review technical documentation, reports, test protocols, and design history file content.

  • Develop proposals for new R&D initiatives in support of capital expenditure planning.

  • Coach and mentor junior engineers in methods, tools, and best practices.

  • Demonstrate and apply Johnson & Johnson’s Credo and Leadership Imperatives in daily work.

Required & Preferred Experience

  • Hands-on experience in catheter design and development, including component or system-level ownership.

  • Experience supporting products through DVT and V&V phases in a regulated environment.

  • Experience working on Class II and/or Class III medical devices.

  • Strong background in mechanical design, device development, and/or manufacturing engineering.

  • Experience partnering with Manufacturing or Operations teams to ensure robust, scalable designs.

  • Working knowledge of design controls, risk management, and regulatory requirements for medical devices.

Qualifications

  • Bachelor’s degree in Mechanical Engineering or a related engineering discipline (advanced degree preferred).

  • Proven experience in mechanical engineering within a medical device R&D environment.

  • Strong analytical, problem-solving, and technical documentation skills.

  • Ability to work independently while contributing effectively to cross-functional teams.

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 law.

Johnson & Johnson is committed to providing an inclusive interview process. If you require an accommodation, please contact the Employee Health Support Center or AskGS for assistance.

Required Skills:



Preferred Skills:

Coaching, Contract Management, Critical Thinking, Design Thinking, Fact-Based Decision Making, Feasibility Studies, Incident Management, Mechanical Engineering, Organizing, Process Oriented, Product Development, Project Management Methodology (PMM), Project Support, Research and Development, SAP Product Lifecycle Management, Technical Credibility, Technical Writing, Vendor Management

The anticipated base pay range for this position is :

$109,000.00 - $174,800.00

Additional Description for Pay Transparency:

Top Skills

Mechanical Engineering
Sap Product Lifecycle Management

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