Find Quality/failure analysis engineer Jobs

Design Quality Assurance Engineer
LGC Diagnostics & Genomics —Tipperary, County Tipperary
- Full-time
- Engineering
- Employee assistance program
Quick apply
11h
Area Business Manager - Southwest England & Wales
BD —Limerick, County Limerick
- €75,900–€115,725 a year
- Engineering
- Master's degree
- Analysis skills
Maintenance Technician (3 Year FTC)
Viatris —Inverin, County Galway
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Veolia Energy Services Ireland Limited. —Clondalkin, County Dublin
- Full-time
- No degree
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Integer Holdings Corporation —Wexford, County Wexford
- Full-time
- Engineering
- English
- Microsoft Office
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Electrical Day Technician
Veolia Energy Services Ireland Limited. —Clondalkin, County Dublin
- Full-time
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Lead Site Reliability Engineer/ Expert
SITA Switzerland Sarl —Letterkenny, County Donegal
- Full-time
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Megasys Safety Specialist
Merck KGaA —Dublin, County Dublin
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Area Business Manager - Southwest England & Wales
BD —Limerick, County Limerick
In addition to technical leadership, the role involves managing cross-functional project teams, applying structured project management methodologies, and…
€75,900–€115,725 a year
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Design Quality Assurance Engineer

LGC Diagnostics & Genomics -
Tipperary, County Tipperary

Quick apply

Job details

Full-time
11 hours ago

Benefits

Employee assistance program

Qualifications

Engineering

Full job description

Company Description

Join Us as a Design & Quality Assurance Engineer in Tipperary!

Are you ready to make a meaningful impact on healthcare?

At LGC Clinical Diagnostics, we’re passionate about improving patient outcomes with products that support accurate and reliable diagnostic results. Now, we’re on the lookout for a Design Quality Engineer to join our dynamic team in Tipperary, Ireland.

This is more than just a job; it’s an opportunity to collaborate with brilliant minds, embrace curiosity, and contribute to innovative solutions—all while living our core values of Passion, Brilliance, Curiosity, and Integrity.

At LGC Clinical Diagnostics (CDx), we're dedicated to advancing science with our comprehensive portfolio of diagnostic quality solutions and component materials. As a member of our team, you'll play a vital role in developing and manufacturing innovative diagnostic products that contribute to accurate and reliable patient outcomes.

We take great pride in upholding high standards in every aspect of our operations. As our Design Quality Engineer, you will be involved in executing projects from initiation to product launch, ensuring adherence to internal policies, regulatory requirements, and Design Control processes.

Job Description

To perform this job successfully, an individual must be able to capably perform each of the following essential functions:

Duties:

Responsible for supporting the Design Control process and ensuring that Design History Files comply with Technopath Clinical Diagnostic (TCD) policies/procedures and applicable regulatory requirements.
Act as the Quality representative on Design Control projects from project initiation through to product launch to ensure compliance to applicable procedures and standards.
Manage and lead the change control process by liaising with impacted areas to ensure timely and compliant implementation and completion.
Work in collaboration with R&D, Labelling, Operations, Validation, Business Development and Supply chain on design control and change control projects.
Review and approve all process validation documentation inclusive of plans, protocols and reports ensuring compliance to applicable procedures and standards.
Responsible for creation and maintenance of Risk Management Files for each product.
Facilitate process and design failure mode and effects analysis meetings.
Responsible for maintaining Design Control and R&D procedures to ensure compliance to regulatory or standard requirements.
Perform Post Market Surveillance activities per the requirements of the applicable procedures and regulations.
Liaise with external customers on change requests.
Provide training and guidance to staff on the requirements of the design control and change control process in TCD.
As required perform internal audits to ensure compliance of TCDs quality management system to the requirements of all applicable requirements.
Perform other related duties as prescribed by the Global Design QA and Risk Manager and Director of Quality Assurance.

Qualifications

Educated to a minimum of degree level in Science/Engineering/QA or related discipline or equivalent.
A minimum of 2 years practical experience required in a quality function or equivalent
Knowledge desirable in relation to risk management; ideally in the IVD or Medical Device industry.
Thorough knowledge of the applicable regulatory requirements.
Knowledge of international regulatory requirements relevant to the business.

Additional Information

Why Join Us?

At LGC Clinical Diagnostics, you’re not just another employee—you’re a valued team member contributing to a better future. We offer:

A collaborative, supportive environment where your ideas matter.
Opportunities to work on impactful projects in the healthcare sector.
A chance to grow professionally while making a tangible difference in people’s lives.

Benefits

25 days holidays
Life assurance & health allowance
Discounts with local and national retailers
Free 24/7 Employee Assistance Programme
Recognition schemes and monetary awards
Great long-term career opportunities

#LGCIJ

Quick apply

Refine Your Search

quality/failure analysis engineer jobs

Design Quality Assurance Engineer

Area Business Manager - Southwest England & Wales

Maintenance Technician (3 Year FTC)

Mechanical Day Technician

NPI Quality Engineer III

Electrical Day Technician

Lead Site Reliability Engineer/ Expert

Megasys Safety Specialist

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