Graduate Quality Engineer – Medical Device GMP Focus (Ireland)

Johnson & Johnson Co.; Limerick; On-site; EUR 32,000 - 45,000; Full time

Job summary

Johnson & Johnson Ireland is inviting high-potential graduates to join its Graduate Programme in Limerick as a Quality Engineer. You will work in a high-volume, fully automated manufacturing environment, supporting quality system design, audits, and compliance while gaining hands-on experience across operations and engineering teams.

The programme offers cross-functional exposure on site, personal development, and a structured pathway to leadership, with an intake in September 2027 and a

Qualifications

• Pursuing a minimum bachelor's level degree in Quality, Mechanical, Production, Manufacturing Engineering or equivalent degree and are due to graduate in 2027.
• Ability to work on own initiative.
• Excellent IT skill e.g., experience in Minitab, Excel reports.
• Ability to apply a scientific approach to problem solving.
• Flexible work ethic.
• Attention to detail.
• Experience in a medical device organisation.

Responsibilities

• Provide quality engineering support within a high-volume, fully automated manufacturing environment.
• Provide product team support for quality system design and audit, compliance assessment, and support of steady state manufacturing processes.
• Utilise medical device industry and process excellence standards in daily quality operations, including GMP and ISO.
• Address and correct product and process complaints.
• Support QA programs and ensure compliance to regulations while attaining operational effectiveness.
• Support and execute upgrades to Quality System and QA programs.

Skills

Own initiative

Attention to detail

Flexible work ethic

Problem solving

Education

Bachelor's degree in Quality/Mechanical/Production/Manufacturing Engineering or equivalent

Tools

Minitab

Excel

Job description

Johnson & Johnson Ireland is inviting high-potential graduates to join its Graduate Programme in Limerick as a Quality Engineer. You will work in a high-volume, fully automated manufacturing environment, supporting quality system design, audits, and compliance while gaining hands-on experience across operations and engineering teams.

The programme offers cross-functional exposure on site, personal development, and a structured pathway to leadership, with an intake in September 2027 and a