Research & Development Engineer | J&J MedTech | Cardiovascular | Ireland

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:
R&D Mechanical Engineering

Job Category:
Scientific/Technology

All Job Posting Locations:
Galway, Ireland, IE013 Ballybritt Galway

Job Description:

Johnson & Johnson MedTech is seeking a Research & Development Engineer based in Galway, Ireland.

Who are we?

At Johnson & Johnson MedTech, 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

Purpose of the role

You will play a pivotal role will play a key role in the development and support of innovative MedTech in a constantly evolving research field.

This position involves supporting new indications for existing products, the development of new neurovascular MedTech products and supporting lifecycle management activities for commercialised products.

You will work cross-functionally with internal teams and external partners to ensure robust product design, regulatory compliance, and effective implementation of product and process improvements.

What to expect:

Provide technical support for regulatory submissions and regional launches; and lead additional engineering studies as the need arises by regional authorities.

Support updates and improvements for existing products through design changes, process optimization, and technical investigations.

Build and update user documentation including procedures, protocols, reports and component specifications

Collaborate with and lead interfaces between cross-functional teams including Supply Chain, Regulatory Affairs, Quality Assurance and Manufacturing to ensure successful project execution.

Contribute to the project team to deliver key objectives while meeting performance, time and cost targets.

Assist in the development and execution of test methods and laboratory experiments.

Support feasibility studies, design verification and validation, and risk management in accordance with applicable regulatory standards.

Contribute to design and development activities for new neurovascular medical devices.

Develop a d...