Product Development Engineer II - Cardiology

Product Development Engineer II

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. We are searching for the best talent for a Product Development Engineer II. This position is an onsite role based in Danvers, MA.

Principal Duties and Responsibilities:

• Apply biomedical, mechanical, and electrical engineering principles to develop medical devices (Impella pump and system).
• Lead and contribute to brainstorms to identify solutions, considering design trade-offs.
• Construct solid models and drawings using GD&T and stack-up analyses
• Fabricate prototypes with support from internal team (machine shop, technicians and designers) 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.
• Effectively communicate activity status, issues, and mitigation plans with collaborators.
• Collaborate to ensure compliance with design controls, company quality policy, and applicable regulatory requirements.

Job Qualifications:

• BS in Mechanical Engineering, Biomedical Engineering, or directly related scientific field
• 2+ years product development experience
• Demonstrated history of performing to meet goals and achieve results
• 3D 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
• Ability to exercise 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 in medical device clinical use, design controls and regulating standards
• Knowledge of cath lab and/or cardiothoracic/vascular surgical environments
• Experience with preclinical evaluation of medical devices
• Solidworks experience

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, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

The anticipated base pay range for this position is $89,000 to $137,000.