R&D Specialist 3

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Job Title: R&D Specialist 3

Company Name:	Johnson & Johnson
Location:	Irvine, CA
Position Type:	Full Time
Post Date:	03/11/2026
Expire Date:	04/10/2026
Job Categories:	Healthcare, Other

Job Description

R&D Specialist 3
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 <a target="_blank" href="https://www.jnj.com">jnj.com</a>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: Project/Program Management GroupJob Sub Function: R&D Project ManagementJob Category:ProfessionalAll Job Posting Locations:Irvine, California, United States of AmericaJob Description:<ul><li>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/medtechWe are searching for the best talent for a R&D Specialist 3 to support our Electrophysiology business. This role will work onsite in our Irvine, CA office.Job Summary:This position supports project teams in the development of electrophysiology catheters and/or related accessories at Biosense Webster. Project coordinator works directly with team to coordinate activities related to new product development and lifecycle.This can include but not limited to sourcing engineering material for new product development, management of the supply chain for new product material, control of inventory, and design control for new product development build activities from onset to submission. Coordinates essential R&D tasks that include contracts with HCPs, trainings of team associates, travel for HCC professionals and other R&D visitors, budget tracking and accruals performance needs.Duties and Responsibilities:</li><li>Function as Project Coordinator for the Device History File of a project team.</li><li>Locate sources for engineering materials and services, obtain quotes and place orders for material and services.</li><li>Maintain design control for new product development build activities.</li><li>Takes an active role in project team/technical projects and initiatives that focus on cost improvement, business continuity, process excellence to enable product development activities.</li><li>Support communication activities regarding R&D initiatives.</li><li>Experience/Education:</li><li>Knowledge and skills to satisfactorily develop the responsibilities of the position.</li><li>4 to 6 years of experience, preferably related to the position.</li><li>University/Bachelors Degree or Equivalent.</li><li>Requirements:</li><li>In depth understanding of specialized area to support new product development and lifecycle manage<ul><li>product structure (Bills of Material, routings, etc.).</li><li>In depth understanding of new product development cost drivers.</li><li>R&D finance and/or contracting process</li></ul></li><li>Ability to work with various engineers & vendors, detailed oriental to track progress</li><li>Ability to participate in a technical team with specialist focus area.</li><li>Must possess excellent communication skills (verbal and written)</li><li>Exceptional aptitude in multitasking</li><li>Ability to utilize office computer programs proficiently.</li><li>Must be detail oriented and highly organized.</li><li>Communicate with other functions within the organization daily to acquire alignment and approvals.</li><li>Manages inventory for clinical investigational materials.</li><li>Maintains traceability for clinical builds and approval for distribution.</li><li>Assist in the development of test reports, generating ECOs and other engineering documentation.</li><li>Responsible for timely presenting of business related issues or opportunities to next management level.</li><li>Windchill PLM system experience is required.</li><li>AutoCAD experience preferred.</li><li>Responsible for ensuring personal and Company compliance with all Federal, State, local and company regulations, policies and procedures.</li><li>Responsible for communicating business related issues or opportunities to next management level.</li><li>For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.</li><li>Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.</li><li>Performs other duties assigned as needed</li></ul>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 <a href="https://www.jnj.com/contact-us/careers" target="_blank">https://www.jnj.com/contact-us/careers</a>. Internal employees contact AskGS to be directed to your accommodation resource.Required Skills: Preferred Skills:Action-Oriented, Agility Jumps, Business Alignment, Business Behavior, Collaborating, Continuous Improvement, Execution Focus, Operations Management, Problem Solving, Process Improvements, Project Management Methodology (PMM), Project Management Office (PMO), Project Reporting, Project Schedule, Quality Control (QC), Research and Development, Stakeholder Engagement The anticipated base pay range for this position is :$92,000.00 - $148,350.00Additional 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

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Johnson & Johnson

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