Senior Engineer, R&D

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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:
Irving, Texas, United States of America, Raritan, New Jersey, United States of America

Job Description:

Johnson & Johnson is recruiting for a Senior Engineer, R&D to join our Aesthetics & Reconstruction group within the MedTech Surgery business located at our Raritan, NJ site with an alternate location of our Irving, TX site.

#Li-Hybrid

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

Position Summary

The Senior Engineer will be responsible for leading and contributing to cross-functional multidisciplinary project teams (R&D, manufacturing, marketing, regulatory, etc.) in the design, development and manufacturing of breast implants, tissue expanders, and related products and processes to fulfill clinical needs within regulatory requirements.

Key Responsibilities


* Lead conceptualization, design and development of new devices or elements of new devices with the intent of commercialization per Quality System Requirements



* Contribute to design/development of product line extensions and product improvements



* Help lead design, development, execution and analysis of results of system, device, component and material tests per laboratory best practices



* Accurately and efficiently translate user and patient needs through design requirements, design specifications and into verified/validated devices and procedures



* Lead verification and validation activities through regulatory clearance and design transfer



* Contribute strongly in the generation of intellectual property



* Collaborate with external (e.g., clinicians) and internal customers (e.g., strategic marketing) to identify user needs and validate device and procedure designs



* Collaborate with clinical, regulatory, quality, manufacturing, etc., to ensure develop...