Product Development Engineer II

• Job title Product Development Engineer II
• Function R&D Product Development
• Sub function Biomedical Engineering
• Category Experienced Engineer, Biomedical Engineering (ST5)
• Location Danvers / United States of America
• Date posted Jul 31 2025
• Requisition number R-024563
• Work pattern Fully Onsite

This job posting is anticipated to close on Aug 30 2025. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.

Description

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

Job Function:

R&D Product Development

Job Sub Function:

Biomedical Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Danvers, Massachusetts, United States of America

Job Description:

Johnson & Johnson is currently seeking a Product Development Engineer II to join our Heart Recovery team located in Danvers, MA.

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 .

Key Responsibilities:

• Build and innovate current medical, technical, and biomedical developments related to company products and heart recovery technologies.

• Support and/or drive sustaining activities of existing product lines, including involvement with Corrective and Preventive Actions.

• Work towards leading product development improvement efforts per plan with some direct supervision. Prepare, present and lead design reviews to attain agreement on projects with peers and cross-functional review teams.

• Develop and update design documentation including component and assembly drawings, article specifications, test protocols, reports, and engineering summaries to support both quality and regulatory documentation. Fabricate prototypes with assistance from junior staff, technical support team (Machine Shop, Technicians and Designers) and suppliers. Maintain accurate documentation of concepts, designs, and processes.

• Resolve producibility issues with internal and external manufacturing partners. Work with internal and external manufacturing partners to ensure producible designs (DFM). Document designs by constructing solid models and drawings using GD&T and stack-up analyses.

• Perform evaluations, design and prototyping using CAD (Solidworks), FEA, 3-D printing to accelerate development and engineering of plastics, ceramic, composite and metallic parts, electromechanical systems, etc.

Qualifications:

Education:

• BS in Mechanical Engineering or directly related scientific field, MS Preferred.

Experience and Skills:

Required:

• 2-3 years experience with Bachelor's degree.

• Ability to communicate ideas and information clearly, effectively, and frequently (oral and written) with stakeholders, project team, local and international.

• Ability to exercise independent judgment in methods, techniques, and evaluation criteria for obtaining results.

• Ability to act independently to resolve methods and procedures.

• Must be proficient in Microsoft Office Suite.

Preferred:

• Product development experience in Class 3 Medical Device engineering

• Advanced degree, MSc/MEng

• Applied understanding of DFM concepts and manufacturing best practices

• Experience in Test Method Validation

• Working knowledge of SAP and Minitab desired.

Other:

• English required

• May require up to 10% travel - US & EU

Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

The anticipated base pay range for this position is $106,250 to $143,750.

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401k).This position is eligible to participate in the Company's long-term incentive program. Employees are eligible for the following time off benefits: Vacation - up to 120 hours per calendar year. Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year. Holiday pay, including Floating Holidays - up to 13 days per calendar year. Work, Personal and Family Time - up to 40 hours per calendar year. For additional general information on Company benefits, please go to: - This job posting is anticipated to close on August 8, 2025. The Company may however extend this time-period, in which case the posting will remain available on to accept additional applications.