R&D Engineer

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 https://www.jnj.com

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:

We are searching for the best talent for a R&D Engineer located in West Chester, PA

Purpose: 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.

In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:


* The R&D Engineer will be responsible for the design and development aspects of a project, participating on cross-functional project teams through all phases of the product life-cycle, and assisting the project leader with planning and executing projects or portions of a project through product launch, commercialization, and post market surveillance.


* Technically lead design and development projects with oversight, and will work closely with the project leader, members of the project core team (marketing, quality, supply chain, manufacturing, regulatory etc.).


* Interacts with design engineers, marketing, quality, supply chain, manufacturing, regulatory affairs, Health Care Professionals, and other functional departments to define and develop product requirements and concepts on new/or existing products.


* Develop layouts and tolerance studies utilizing geometric dimensioning and tolerancing (GD&T), and will participate in performing design evaluations (such as FEA, simulated use testing, dry labs and wet tissue/cadaver labs etc.).


* Solve design problems utilizing CAD techniques, rapid and conventional prototyping and other available technologies.


* Development and execution of design verification/validation plans, test methods and protocols, and will support regulatory processes for global registration efforts. 


* Performs the required activities and generate the appropriate documents to ensure compliance with MDR; FDA Design Control regulations, and to support 510(k) submissions or IDE clinical s...