PD Engineer I- Cardiology at Johnson & Johnson MedTech
John Johnson & Johnson MedTech 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. The Company maintains highly competitive, performance-based compensation programs and offers a comprehensive benefits package.
Job Overview
We are developing the next generation of smarter, less invasive, more personalized treatments for cardiovascular disease. This onsite role is based in Danvers, MA, and focuses on product development for the Impella pump and system.
Principal Duties and Responsibilities
- Apply biomedical, mechanical, and electrical engineering principles to develop medical devices (Impella pump and system).
- Lead and contribute to brainstorming sessions to identify design solutions and evaluate trade-offs.
- Construct solid models and drawings using GD&T, stack-up analyses, and prototype fabrication with internal teams and external suppliers.
- Develop, validate, and execute test methods for design characterization and verification.
- Work with internal and external manufacturing partners to ensure producible designs (DFM).
- Prepare and present design reviews, ensuring the technical integrity of the product design.
- Address technical and programmatic risks, ensuring effective risk identification, assessment, and mitigation.
- Communicate activity status, issues, and mitigation plans with collaborators.
- Ensure compliance with design controls, company quality policy, and applicable regulatory requirements.
Job Qualifications
BS in Mechanical Engineering, Biomedical Engineering, or a related scientific field.3-D modeling experience.Experience applying statistical analysis (Six Sigma and / or Design for Six Sigma, tolerance analysis).Strong problem-solving skills and experience with root cause investigations.Independent judgment in methods, techniques, and evaluation criteria for obtaining results.Willingness and ability to travel domestically and to the EU, up to 10% of the time, in support of role responsibilities.Preferred Qualifications
Master of Science degree.Medical device product development experience.Knowledge of medical device clinical use, design controls, and regulatory standards.Knowledge of cath lab and / or cardiothoracic / vascular surgical environments.Experience with preclinical evaluation of medical devices.SolidWorks experience.Compensation and Benefits
Base pay range : $74,000 to $119,600. Eligible for annual performance bonus and long-term incentive program. Comprehensive benefits include medical, dental, vision, life insurance, short- and long-term disability, business accident, group legal insurance, 401(k) with company match, paid time off, and holidays.
Application Period
This posting will close on September 15, 2025. The Company may extend this time-period, in which case the posting will remain available to accept additional applications.
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