R&D Analyst, PMO - JJMT Electrophysiology

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 https://www.jnj.com

Job Function:

Project/Program Management Group

Job Sub Function:

R&D Project Management

Job Category:

Professional

All Job Posting Locations:

Irvine, California, United States of America

Job Description:

Johnson & Johnson MedTech, Electrophysiology, is recruiting an R&D Analyst, PMO to join our R&D team in Irvine, California.  This role is fully on-site at the Irvine location.

  

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 https://www.jnj.com/.   

  

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 

Key Responsibilities:

• Coordinates daily activities of project teams and provides assistance whenever needed.
• Assists with the development of advanced materials, process improvements, risk management, and/or mechanical testing.
• Preforms strategies and methods to improve operations in productivity, standards, and profits.
• Prepares reports and documents to ensure accurate and timely reporting of program status throughout its life cycle.
• Develops basic process improvements that lead to improvements in productivity, quality, and cost.
• Coordinates development and quality assurance resources for successful completion of projects.
• Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.

Qualifications:

Education

• Bachelor’s degree in Engineering, Life Sciences, Business, or related field
• Bonus: Project management coursework, certifications (CAPM, PMP, or equivalent)

​

Experience

• 2–4 years of experience in project coordination, ideally in medical device, biotech, or pharma R&D.
• Exposure to regulated environments (FDA, ISO 13485, EU MDR) and understanding of design controls.
• Experience supporting cross-functional teams (engineering, clinical, regulatory, quality, operations).
• Familiarity with project tracking tools (MS Project, Smartsheet, Jira, or equivalent).

Technical / Functional Skills

• Strong skills in document control, scheduling, and meeting coordination.