2026 Graduate Quality 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:
Supply Chain Engineering

Job Sub Function:
Quality Engineering

Job Category:
Scientific/Technology

All Job Posting Locations:
Limerick, Ireland

Job Description:

Role Title: Graduate Quality Engineer

Intake: September 2026
Location: Limerick

About the Johnson & Johnson Graduate Programme:

The Graduate Programme is a collaborative programme across the Johnson & Johnson Campus Ireland Sites.

It is aimed at high potential individuals who, when given the right tools, are empowered to proactively take responsibility, effect change and make a positive contribution to their teams and the business.

The Successful Candidate will have the opportunity to: 


* Develop relevant technical skills within their area of expertise.


* Cross functional exposure both on site and within Campus Ireland.


* Regular one to ones and feedback to support your on-going development.


* Personal development and effectiveness training.


* Skills development in influencing & communication.


* Project and Project Management experience.


* Introduction to new and innovative technologies.


* Exposure to Senior Management Team.


* Continuous professional development program with a recognised qualification.

Roles & Responsibilities

The Graduate Quality Engineer position is focused on providing quality engineering support within a high volume, fully automated manufacturing environment.


* Provides product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes


* Utilizes medical device industry and process excellence standards in daily quality operations, including good manufacturing practices (GMP) and international organization for standardization (ISO).


* Addresses and corrects product and process complaints.


* Responsible for supporting the activities of Operations/Engineering/information management in building quality into our products and assuring compliance to the pertinent regulations while at the same time attaining operational effectiveness


* Supports and executes upgrades to Quality System


* Support QA programs in assuring compliance to the pertinent regulation


* Support lead cost and technical improvements under the departments’ continuous improvement program.


* Project Management - provide timely and accurate reporting on project activities.


* Actively particip...