
R&D Analyst, PMO - JJMT Electrophysiology
- Irvine, CA
- $74,000-119,000 per year
- Permanent
- Full-time
- 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.
- 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).
- Strong skills in document control, scheduling, and meeting coordination.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
- Ability to prepare project status reports, dashboards, and presentations for leadership.
- Knowledge of risk management tools and change control processes.
- Comfort with budget tracking, resource allocation, and milestone tracking.