Sustaining R&D Engineer

Job title Sustaining R D Engineer Function R D Product Development Sub function Biomedical Engineering Category Engineer, Biomedical Engineering (ST4 - N23) Location West Chester / United States of America Date posted May 11 2026 Requisition number

R-073907

Work pattern Hybrid Work This job posting is anticipated to close on May 19 2026. 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 jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

R D Product Development Job Sub Function:

Biomedical Engineering Job Category:

Scientific/Technology All Job Posting Locations:

West Chester, Pennsylvania, United States of America Job Description:

About MedTech Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness.

Learn more at https:

//www.jnj.com/medtech Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes. We are searching for the best talent for a Sustaining R D Engineer . The Sustaining R D Engineer helps lead the design and development of new implants and instrumentation and/or support in-market products through their product life-cycle within a cross-functional project team. This includes communication with customers, e.g. Health Care Professionals and marketing, understanding of clinical issues, defining the design parameters, and ensuring the product, which is provided to the customer, meets the functional requirement.

Key Responsibilities:

Lead and execute design and development activities across the product life cycle, from concept through commercialization and post‑market support, as part of cross‑functional project teams. Technically support and partially lead projects with oversight, partnering closely with the Project Leader and Project Core Team (Marketing, Quality, Manufacturing, Supply Chain, Regulatory). Define and develop product requirements and design concepts through collaboration with internal teams and Health Care Professionals. Create CAD designs, layouts, and tolerance analyses using GD solve design challenges using prototyping, FEA, and simulated‑use, dry, and wet lab testing. Develop and execute design verification and validation plans, methods, and protocols; analyze results and author technical reports. Ensure compliance with

MDR, FDA

Design Controls, and global regulatory requirements, including support of 510(k) submissions, IDE studies, audits, and inspections. Apply Six Sigma and structured problem‑solving methodologies to resolve complex technical issues. Support supplier, manufacturing, and operations teams to optimize designs for manufacturability, assembly, cost improvement, and production transfers. Engage Health Care Professionals to define user needs, evaluate prototypes, and support clinical follow‑up while maintaining awareness of surgical trends. Support intellectual property reviews for freedom to operate and assist with budget‑related responsibilities as applicable. Participate in complaint investigations, field actions, non‑conformance remediation, and other quality and compliance‑related activities. Promote and adhere to the highest standards of professionalism, ethics, safety, and compliance in accordance with company policies and regulations. Perform special projects and additional duties as assigned.

Requirements:

Education Bachelor's degree in Engineering or related discipline required. Mechanical Engineering degree or demonstrated mechanics focus preferred. Required Minimum of 2 years of experience in design and development of medical devices, mechanical products, or biomechanical systems. Mechanical design experience, including exposure to design controls and development engineering. Strong understanding of mechanical design principles, materials, manufacturing processes (particularly machining), tolerancing, drafting standards, and GD&T. Demonstrated ability to execute project responsibilities, manage multiple priorities, and overcome technical challenges. Strong problem‑solving, decision‑making, and root cause analysis skills. Effective written and verbal communication skills, including the ability to communicate technical concepts across functions and with Health Care Professionals. Proficiency with Microsoft Office (Word, Excel, PowerPoint). Ability to work with wet tissue/cadaver labs and within an operating room environment. Ability to travel at least 10% Preferred Knowledge of biomechanics, anatomy, and biology. Familiarity with orthopedic or TECA product portfolios. Experience with MDR/FDA regulations, including 510(k) submissions and/or IDE clinical studies. Proficiency with CAD tools (e.g., Creo/ProE). Six Sigma Green Belt certification. Experience with design verification/validation, DFMEA/PFMEA, and process validation. Experience with implantable medical devices and/or plastic injection molding and design for manufacturability. Prior project management experience. Exposure to GMP, QSR, ISO, and good documentation practices (GDP). 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. #

LI-Hybrid Required Skills:

Preferred Skills:

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