49 Quality Assurance jobs in Ireland
Quality Technician
Ballymena, Ulster
Wrightbus
Job Viewed
Job Description
Job type: Permanent Location: Wrightbus Closing date: Monday 11 Aug 2025 08:00 We reserve the right to close this vacancy early if we receive sufficient applications from suitably qualified and experienced candidates. We therefore encourage early applications. Candidates who applied for this role within the past six months and were not successful should wait at least six months before reapplying. All applicants must hold valid right to work in the UK. Please be aware that we are unable to provide visa sponsorship for this position now or in the future. The Job Summary: Wrightbus is the fastest growing production company in Europe, and we are looking for a Quality Technician. This role is crucial in ensuring all buses manufactured meet company and regulatory quality standards. Responsibilities include inspecting components, assemblies, and finished products for defects, enforcing quality control processes, and collaborating with production teams to maintain high workmanship standards. The Role: Conduct inspections of materials, in-process production, and finished buses to ensure compliance with specifications. Perform functional and safety tests on electrical, mechanical, and structural components of buses. Use measuring tools and testing equipment to verify dimensions, tolerances, and performance criteria. Identify and document defects, deviations, and non-conformities, and ensure corrective actions are taken. Ensure compliance with company quality standards, customer specifications, safety regulations, and industry requirements. Assist in the development and enforcement of standard operating procedures (WMPs) for quality assurance. Conduct audits and assessments of manufacturing processes to identify areas for improvement. Maintain detailed records of inspections, test results, and corrective actions taken. Prepare quality reports and present findings to supervisors and production teams. Assist in root cause analysis and the development of preventive measures. Evaluate and approve new/existing suppliers through supplier audits. Ensure all rectification/rework meets agreed standards. Implement relevant processes and procedures within the QMS. Support continuous improvement initiatives by providing feedback on quality trends and recurring issues. Communicate with all departments to eliminate defects at the source. Identify root causes of any relevant issues and implement solutions with operators, or other departments, to prevent re-occurrence. Identify any operator training needs required to meet WMP/quality standards and refer to Level 4 operators and/or Safety Auditors to undertake training. Where necessary, complete the relevant training record. Provide feedback on any of the issues above to allow Quality documentation to be updated and to carry forward lessons learned. The Requirements Minimum of 5 GCSE's grade C and above OR An apprenticeship qualification 1 Year previous quality inspection experience in manufacture or fabrication Ability to identify root causes and implement corrective actions Strong understanding of quality control processes, inspection techniques, and defect analysis. Working knowledge of quality procedures and practices Ability to interpret engineering drawings and wiring diagrams The Benefits: Discretionary bonus Life Insurance Medicash scheme Discount with local businesses e.g. Galgorm Spa Resort and McAtamney's. Free car parking Canteen Career progression Professional development Flexitime #wbstaff To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process click the Continue to Application or Login/Register to apply button below.
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Quality Assurance Analyst
Dublin, Leinster
Diageo
Posted 1 day ago
Job Viewed
Job Description
**Job Description :**
**Quality Assurance Analyst**
**St. James's Gate Brewery, Dublin**
**12 Month Fixed Term Contract**
**Closing Date: 22nd** **August 2025**
**About Us**
With over 200 brands sold in nearly 180 countries, we're the world's leading premium drinks company. Bring your passion and use your curiosity as you explore, collaborate, and innovate to build brands consumers love. Together with passionate people from all over the world, you'll test new ideas, learn and grow, and unlock a brighter, more exciting future.
Join us to create a career worth celebrating!
**About the Function**
Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo's 30,000+ people work in Supply Chain and Manufacturing. It's an intricate and sophisticated operation that's the product of logistical, manufacturing, and technical collaborations.
Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We're committed to realising our 'Society 2030: Spirit of Progress' goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we'll help you to thrive in our inclusive culture.
**About the Role**
We are looking for a Quality Assurance Analyst to join our team, providing a wide range of laboratory analysis to support our brewing and project teams. This role plays a key part in driving the Quality Agenda on-site, supporting projects, developing new analytical testing methods and ensuring high standards across all lab operations.
You will work closely with production teams across the brewery, reporting directly to the Quality Manager and acting as a key liaison between quality and operational teams to ensure accurate, timely data and continuous improvement of laboratory processes.
**Purpose of the role:**
+ Provide accurate and repeatable analytical data to the brewing teams in a timely manner.
+ Understand the relevance of analysis at each stage of the brewing process and promptly report any out-of-spec results to the Brewing Shift Manager.
+ Analyse trends in laboratory instrument performance, troubleshoot deviations and diagnose root causes.
+ Provide technical input and coaching to production teams when issues arise.
+ Support all aspects of the Quality Agenda on site, including projects and the development of new analytical tests.
**Key Responsibilities:**
+ Ensure asset care of all laboratory instruments, maintaining the lab to a high operational standard.
+ Maintain and calibrate instruments, prepare standards and analytical reagents required for testing.
+ Conduct routine sample analysis as required and coordinate external sample testing, including monthly submissions and result recording.
+ Operate and calibrate the Thermofisher for Poly, FAN, Iron and Calcium analysis, including introducing ABV analysis for pure brew.
+ Perform Atomic Absorption Spectroscopy (AAS) for yeast zinc and wort magnesium analysis, and GC-MS pyrazine analysis when requested.
+ Handle site-wide sampling, particularly in support of project-related work.
+ Deliver accurate analytical data on time, ensuring all Quality Sample Plans are met.
+ Work to safe systems of operation, conducting risk assessments of laboratory processes.
+ Take ownership of your training and development needs to maintain high technical capability.
+ Support the development and implementation of the site's Quality & Food Safety Strategy, contributing to FSSC 22000, ISO 9000 and FEMAS certification compliance.
+ Lead and support initiatives to enhance lab capabilities and reduce operational costs.
This is a hands-on role ideal for someone who thrives on problem-solving, process improvement and delivering precise, reliable analytical data to support brewing excellence.
Additionally, this role entails providing long-term sick cover for analytical and micro lab duties, so it is important that the successful candidate is flexible around business requirements at short notice. This would potentially cover day, night and weekend shifts.
**About You**
We're looking for someone with a passion for quality, continuous improvement, and scientific excellence, who can work collaboratively to support our teams. If you're motivated to make an impact and thrive in a hands-on laboratory environment, this could be the perfect role for you.
You'll bring:
+ A science degree in a relevant scientific subject.
+ An IBD brewing qualification (desirable, but not essential).
+ Knowledge of statistical techniques, including Statistical Process Control (SPC).
+ Strong problem evaluation and solving skills, with the ability to think critically and deliver solutions.
+ Excellent organisational skills and great attention to detail.
+ A team-focused approach, contributing positively to collaborative working and shared goals.
**Working with Us**
Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this.
We embrace diversity in the broadest possible sense. This means that you'll be welcomed and celebrated for who you are just by being you. You'll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more.
Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world.
**Feel inspired? Then this may be the opportunity for you!**
**Worker Type :**
Regular
**Primary Location:**
St James Gate
**Additional Locations :**
**Job Posting Start Date :**
2025-08-06
With over 200 brands sold in more than 180 countries, we're the world's leading premium drinks company. Every day, over 30,000 talented people come together at Diageo to create the magic behind our much-loved brands. From iconic names to innovative newcomers - the brands we're building are rooted in culture and local communities. Our ambition is to be one of the best performing, most trusted and most respected consumer products companies in the world.
Our founders, such as Arthur Guinness, John Walker, and Charles Tanqueray, were visionary entrepreneurs whose brilliant minds helped shape the alcohol industry. And through our people, their legacy lives on. Join us, and you'll collaborate with talented people from all corners of the world. Together, you'll innovate and push boundaries, shaping a more inclusive and sustainable future that we can all be proud of.
With diversity at our core, we celebrate our people's unique passions, commitments and specialist skills. Because when varied voices, mindsets, and personalities come together, great ideas are born. In our supportive culture, your voice will be heard and you'll be empowered to be you. Just bring your ambition, curiosity and ideas, and we'll celebrate your work and help you reach your fullest potential.
**DRINKiQ**
What's your DRINKiQ? Take our quiz to understand how alcohol is made and explore the effects of drinking. You can discover everything you need to know at DRINKiQ (
**Quality Assurance Analyst**
**St. James's Gate Brewery, Dublin**
**12 Month Fixed Term Contract**
**Closing Date: 22nd** **August 2025**
**About Us**
With over 200 brands sold in nearly 180 countries, we're the world's leading premium drinks company. Bring your passion and use your curiosity as you explore, collaborate, and innovate to build brands consumers love. Together with passionate people from all over the world, you'll test new ideas, learn and grow, and unlock a brighter, more exciting future.
Join us to create a career worth celebrating!
**About the Function**
Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo's 30,000+ people work in Supply Chain and Manufacturing. It's an intricate and sophisticated operation that's the product of logistical, manufacturing, and technical collaborations.
Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We're committed to realising our 'Society 2030: Spirit of Progress' goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we'll help you to thrive in our inclusive culture.
**About the Role**
We are looking for a Quality Assurance Analyst to join our team, providing a wide range of laboratory analysis to support our brewing and project teams. This role plays a key part in driving the Quality Agenda on-site, supporting projects, developing new analytical testing methods and ensuring high standards across all lab operations.
You will work closely with production teams across the brewery, reporting directly to the Quality Manager and acting as a key liaison between quality and operational teams to ensure accurate, timely data and continuous improvement of laboratory processes.
**Purpose of the role:**
+ Provide accurate and repeatable analytical data to the brewing teams in a timely manner.
+ Understand the relevance of analysis at each stage of the brewing process and promptly report any out-of-spec results to the Brewing Shift Manager.
+ Analyse trends in laboratory instrument performance, troubleshoot deviations and diagnose root causes.
+ Provide technical input and coaching to production teams when issues arise.
+ Support all aspects of the Quality Agenda on site, including projects and the development of new analytical tests.
**Key Responsibilities:**
+ Ensure asset care of all laboratory instruments, maintaining the lab to a high operational standard.
+ Maintain and calibrate instruments, prepare standards and analytical reagents required for testing.
+ Conduct routine sample analysis as required and coordinate external sample testing, including monthly submissions and result recording.
+ Operate and calibrate the Thermofisher for Poly, FAN, Iron and Calcium analysis, including introducing ABV analysis for pure brew.
+ Perform Atomic Absorption Spectroscopy (AAS) for yeast zinc and wort magnesium analysis, and GC-MS pyrazine analysis when requested.
+ Handle site-wide sampling, particularly in support of project-related work.
+ Deliver accurate analytical data on time, ensuring all Quality Sample Plans are met.
+ Work to safe systems of operation, conducting risk assessments of laboratory processes.
+ Take ownership of your training and development needs to maintain high technical capability.
+ Support the development and implementation of the site's Quality & Food Safety Strategy, contributing to FSSC 22000, ISO 9000 and FEMAS certification compliance.
+ Lead and support initiatives to enhance lab capabilities and reduce operational costs.
This is a hands-on role ideal for someone who thrives on problem-solving, process improvement and delivering precise, reliable analytical data to support brewing excellence.
Additionally, this role entails providing long-term sick cover for analytical and micro lab duties, so it is important that the successful candidate is flexible around business requirements at short notice. This would potentially cover day, night and weekend shifts.
**About You**
We're looking for someone with a passion for quality, continuous improvement, and scientific excellence, who can work collaboratively to support our teams. If you're motivated to make an impact and thrive in a hands-on laboratory environment, this could be the perfect role for you.
You'll bring:
+ A science degree in a relevant scientific subject.
+ An IBD brewing qualification (desirable, but not essential).
+ Knowledge of statistical techniques, including Statistical Process Control (SPC).
+ Strong problem evaluation and solving skills, with the ability to think critically and deliver solutions.
+ Excellent organisational skills and great attention to detail.
+ A team-focused approach, contributing positively to collaborative working and shared goals.
**Working with Us**
Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this.
We embrace diversity in the broadest possible sense. This means that you'll be welcomed and celebrated for who you are just by being you. You'll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more.
Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world.
**Feel inspired? Then this may be the opportunity for you!**
**Worker Type :**
Regular
**Primary Location:**
St James Gate
**Additional Locations :**
**Job Posting Start Date :**
2025-08-06
With over 200 brands sold in more than 180 countries, we're the world's leading premium drinks company. Every day, over 30,000 talented people come together at Diageo to create the magic behind our much-loved brands. From iconic names to innovative newcomers - the brands we're building are rooted in culture and local communities. Our ambition is to be one of the best performing, most trusted and most respected consumer products companies in the world.
Our founders, such as Arthur Guinness, John Walker, and Charles Tanqueray, were visionary entrepreneurs whose brilliant minds helped shape the alcohol industry. And through our people, their legacy lives on. Join us, and you'll collaborate with talented people from all corners of the world. Together, you'll innovate and push boundaries, shaping a more inclusive and sustainable future that we can all be proud of.
With diversity at our core, we celebrate our people's unique passions, commitments and specialist skills. Because when varied voices, mindsets, and personalities come together, great ideas are born. In our supportive culture, your voice will be heard and you'll be empowered to be you. Just bring your ambition, curiosity and ideas, and we'll celebrate your work and help you reach your fullest potential.
**DRINKiQ**
What's your DRINKiQ? Take our quiz to understand how alcohol is made and explore the effects of drinking. You can discover everything you need to know at DRINKiQ (
This advertiser has chosen not to accept applicants from your region.
0
Quality Assurance Officer
Kildare, Leinster
Nua Healthcare
Posted 4 days ago
Job Viewed
Job Description
Job Summary Nua Healthcare Services (Nua) is one of Ireland's leading Private Healthcare Providers, specialising in Residential and Supported Living Services, to both Children and Adults with a range of complex support needs. We are seeking applications from energetic and enthusiastic individuals to join our team for the above positions. The successful candidate will be afforded all necessary training and development in line with the role. Candidates must be highly motivated and creative, with a passion for engaging with Service Users on a daily basis. Candidates will contribute to enriching the lives of our Service Users. Job Objectives We are seeking a dedicated and experienced Quality Assurance Officer to join our dynamic team at Nua Healthcare. We have several positions available, within the areas of Kildare, Meath and Dublin The post holder will ensure compliance, both operational and legislative across all areas of the business along with conducting audits across all areas of the business. Submit reports, agree corrective actions, and support Teams to action any approved recommendations regarding business activities. This will include the following on a day-to-day basis: Live our Mission, Vision and Values. Support the development and implementation of the Internal Audit department and its policies and procedures. Support the design of audit programs and execute audits to verify compliance with legislation, regulation, standards and company policies and procedures. Communicate Audit findings to key Management and follow up on audit issues. Analyzing large amounts of data. Implementation of any recommendations approved. Undertake continuous improvement programs in conjunction with Operations and Clinical Services departments. Develop and maintain an excellent knowledge of all business activities. Develop and maintain excellent knowledge of accepted professional standards such as HIQA. standards, HSE, HSA and all relevant legislation regarding our business. Assist Centre Management regarding compiling and presenting reports as required (Reg 23 Six Month Visit & Annual Report). Maintain strict confidentiality in relation to staff and service users. Please note: This role requires travel nationwide Skills Requirement Qualifications: A Third Level Qualification in Healthcare / Social Studies (or suitable equivalent relevant qualification). Knowledge: Knowledge of standards and legislation relevant to the area. Some (demonstrable) previous knowledge of: Standards and legislation relevant to the health and social care sector. Quality Frameworks / Quality Improvement Tools. Health & Safety Management and associated legislation. Experience: Demonstrable previous experience in a similar role. Experience of / with people with additional and/or complex needs. Skills: High standard of IT literacy. Excellent problem solving and decision-making skills under pressure, ability to work on your own initiative. Excellent organisational skills / self-motivated / self-starter. Excellent verbal, written communication, and IT skills. Full Clean Drivers Licence Benefits Company Pension Company Vehicle Continuous Professional Development Fantastic development & career opportunities Life Assurance/Death-in-Service Paid Maternity/Paternity Leave Education Assistance Employee Assistance Programme (EAP) Bike to work Scheme. Refer/Retain a friend bonus. Discounts with Retailers - Nationwide Attachment(s): Quality Assurance- Job To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process click the Apply button below to Login/Register.
This advertiser has chosen not to accept applicants from your region.
1
Quality Assurance Technologist
Dunboyne, Leinster
Amicus Recruitment
Posted 5 days ago
Job Viewed
Job Description
About the Role My client, an established business in the pet nutrition industry, is seeking a Quality Assurance Technologist to join their team in Co. Meath. This is a hands-on role where you will be instrumental in the day-to-day operations of the Quality Assurance department. You'll be responsible for maintaining the company's Quality Management System, ensuring all products meet strict food safety standards, and driving a strong food safety culture throughout the organization. You'll also play a key role in product inspections, testing, and new product development. Key Responsibilities Ensure full compliance with company procedures, current legislation, and regulatory requirements. Work closely with customer and supplier technical departments. Support new product development, from ingredient selection to final product. Manage and maintain the Quality Management System and HACCP plan. Monitor and report on key performance indicators (KPIs), investigating any failures and implementing corrective actions. Investigate non-conformances, deviations, and customer complaints, ensuring effective corrective actions are in place. Prepare the site for all audits and ensure timely resolution of any findings. Conduct internal audits, inspections, and product traceability exercises. Assist with continuous improvement initiatives. Qualifications and Skills A degree in Food Science or a related field. Previous experience in a food manufacturing environment. Proficiency in MS Office. Excellent attention to detail and the ability to understand complex standards and specifications. A disciplined and methodical approach to work.
This advertiser has chosen not to accept applicants from your region.
2
Quality Assurance Specialist
Cork, Munster
Catalyx
Posted 5 days ago
Job Viewed
Job Description
Catalyx is seeking a Quality Assurance Specialist to join our team and work on our customer site in Cork. This role operates on a rotating weekly shift pattern, alternating between morning and evening shifts. Who We Are: Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services R&D, production, packaging, and delivery processes-globally-with a sophisticated blend of products, technologies, and lifecycle services. The company was formed in 2022 after CXV Global (Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies joined forces. For over three decades, Catalyx's partnership-based culture has helped organizations in production-intense, highly regulated industries optimize their operational efficiency, performance, and safety. To learn more about the company's experience and comprehensive suite of capabilities and solutions, visit . The Role: Catalyx is a trusted partner in delivering world-class lifecycle services to regulated and high-risk end markets. With a relentless commitment to innovation and excellence, we partner with life science and other highly regulated organisations, to empower them to enhance efficiency, and drive success. As part of this commitment, we are continuously developing our on-site teams to support the advancement of customer operations. Responsibilities: Provide quality oversight across various production stages, including material inspection, in-process control, and product readiness activities. Assemble and review documentation to support product disposition, working closely with operational and quality colleagues to meet release timelines. Support packaging operations by conducting visual inspections and ensuring process adherence during routine activities. Collaborate with cross-functional teams (Manufacturing, Quality Control, Supply Chain, Engineering, etc.) to resolve day-to-day queries and issues efficiently. Contribute to the maintenance and improvement of quality systems through change control, deviation management, and CAPA oversight. Conduct documentation reviews such as batch records, SOPs, and WI updates, ensuring alignment with regulatory and internal standards. Participate in the preparation of periodic quality reports and metrics, supporting trend identification and ongoing improvement. Engage in internal audits and readiness assessments to ensure site and process compliance. Provide knowledge-sharing and informal coaching on quality processes to enable operational teams to work effectively within GMP frameworks. Support project-based work and initiatives aimed at process enhancement and improved compliance practices. Review and approve manufacturing inputs and documents to ensure compliance with release criteria. Requirements: Bachelor's degree in a scientific or technical discipline. Minimum 3 years' experience in a Quality or GMP-related role within the pharmaceutical, biotech or related regulated sector. Familiarity with batch documentation, quality systems, and regulatory expectations (e.g., FDA, EMA). Ability to analyse issues, identify appropriate corrective actions, and escalate where necessary. Experience supporting or interacting with packaging or material management processes is beneficial. Strong written and verbal communication skills; confident working in a collaborative environment. Competence with Microsoft Office tools, particularly Excel and Word. Organised, detail-focused, and capable of managing multiple priorities. Comfortable working independently within defined parameters, and adaptable to shifting project needs Why Join Catalyx? At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone. At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.
This advertiser has chosen not to accept applicants from your region.
3
Quality Assurance Manager
Dublin, Leinster
ICDS Group
Posted 5 days ago
Job Viewed
Job Description
Quality Assurance & Continuous Improvement Manager Location:Dublin 3 (Head Office) €80,000-€90,000 + Benefits A leading international construction company is seeking a Quality Assurance & Continuous Improvement Manager to join their head office team in Dublin. This role will oversee quality systems across a wide range of major projects, ensuring regulatory compliance and driving best practices throughout the business. Key Responsibilities: Manage and maintain the companys Quality Management System in line with ISO 9001 and EU Construction Product Regulations Develop and implement project-specific quality plans, inspection and test plans, and documentation templates Lead internal and external audits, ensuring corrective and preventative actions are tracked and closed out Collaborate with project teams to embed quality standards from project set-up to final handover Deliver training and guidance to teams across the business on quality processes and requirements Promote continuous improvement by identifying opportunities, leading initiatives, and sharing lessons learned Liaise with consultants, site teams, and supply chain partners to ensure quality expectations are met Ensure full compliance with Irish and European building regulations and relevant legislation Requirements: Degree in Construction, Engineering, or related discipline Minimum 10 years experience in a quality-focused role within the construction industry Strong knowledge of ISO 9001, CE marking, and EU/regulatory compliance Experience implementing and managing QMS across multiple projects Excellent leadership, communication, and organisation skills Willingness to travel to project sites across Ireland and Europe This is an exciting opportunity to take on a strategic role in a well-established company offering a competitive salary, benefits, and genuine long-term progression. Skills: Quality Assurance Quality Control ISO 9001
This advertiser has chosen not to accept applicants from your region.
4
Quality Assurance & Engineering
D18 Dublin, Leinster
Fulcrum Digital
Posted 7 days ago
Job Viewed
Job Description
Overview: We are the global technology company behind the world’s fastest payments processing network. We are a vehicle for commerce, a connection to financial systems for the previously excluded, a technology innovation lab, and the home of Priceless®. We ensure every employee has the opportunity to be a part of something bigger and to change lives. We believe as our company grows, so should you. We believe in connecting everyone to endless, priceless possibilities. Our team within Client's The Services team is a key differentiator for Client's, providing the cutting-edge services that are used by some of the world's largest organizations to make multi-million dollar decisions and grow their businesses. Focused on thinking big and scaling fast around the globe, this agile team is responsible for end-to-end solutions for a diverse global customer base. Centered on data-driven technologies and innovation, these services include payments-focused consulting, loyalty and marketing programs, business Test & Learn experimentation, and data-driven information and risk management services. Advanced Analytics Program: Within the Services Technology Team, the Targeting Analytics program is a relatively new program that is comprised of a rich set of products that provide accurate perspectives on Credit Risk, Portfolio Optimization, and Ad Insights. Currently, we are enhancing our customer experience with new user interfaces, moving to API-based data publishing to allow for seamless integration in other Client's products and externally, utilizing new data sets and algorithms to further analytic capabilities, and generating scalable big data processes. We are looking for an innovative software quality engineer who can design and execute test plans for key full-stack features and our data pipeline and thrive in a fast-paced, agile team. The range of work you encounter varies from writing automated tests to ensuring analytical accuracy and beyond. This individual will be part of a large, cross-functional team and collaborate closely with our Customer Experience, Product Development, and Engineering teams. Engineers work in small, flexible teams. Every team member contributes to designing, building, and testing features. The range of work you will encounter varies from building intuitive, responsive UIs to designing backend data models, architecting data flows, and beyond. There are no rigid organizational structures, and each team uses processes that work best for its members and projects. Here are a few examples of products in our space: • Portfolio Optimizer (PO) is a solution that leverages Client's data assets and analytics to allow issuers to identify and increase revenue opportunities within their credit and debit portfolios. • Audiences uses anonymized and aggregated transaction insights to offer targeting segments that have high likelihood to make purchases within a category to allow for more effective campaign planning and activation. • Credit Risk products are a new suite of APIs and tooling to provide lenders real-time access to KPIs and insights serving thousands of clients to make smarter risk decisions using Client's data.
RequirementsRole: o Play a crucial part in helping drive Quality to help build and ship better products. o Drive Quality Engineering methodologies and help build high quality software. o Create, manage and maintain test cases, and test data. o Develop and execute a) functional/integration tests, b) data quality tests, c) automated tests, and d) performance tests for APIs and web apps, o Collaborate closely with our development teams to enhance our existing software development processes. o Partner with developers to improve and automate test and release processes. o Help make Quality an integral part of the development process. All About You: o 3+ years of experience as a Software Quality Engineer, Software Engineer in Test, Test Automation engineer, Developer or related occupation, leveraging software QA tools and processes. o Experience with a variety of different testing techniques such as UI testing, Automated testing, Test driven development strategies etc. o Must be experienced with testing data intensive applications and data quality testing o Must have strong expertise of using Selenium Web Driver (Java 8) for automated GUI testing. o Expertise in using Postman/SOAPUI/Blazemeter Pro for automated API testing and creating automated regression packs. o Proven experience (recent) working in a continuous integration environment with hands on experience of configuration of Jenkins builds and executing tests using Jenkins. o Full understanding of test and project delivery life cycles. o Ability to analyze application logs and assist engineers by utilizing basic debugging techniques o Have experience with defect/requirements management tools. o Have hands on experience working with version control tools such as Subversion and GIT. o Excellent communication skills,
This advertiser has chosen not to accept applicants from your region.
5
Quality Assurance Technician, Intermediate
Clonmel, Munster
Abbott
Posted 19 days ago
Job Viewed
Job Description
**Abbott in Ireland**
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Ireland Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Our broad line of vascular devices-which includes vessel closure, endovascular and coronary technologies-are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
**PURPOSE OF THE JOB**
Provides technical assistance to engineering to support
manufacturing efforts by implementing corrective and preventative actions. Assists engineers in developing methods and procedures to control or improve manufacturing processes.
**MAJOR RESPONSIBILITIES**
+ Assists engineering in providing manufacturing support bylearning to analyse data and identify manufacturing issues and trends. May also train operators on basic processes and engineering changes, and perform operator certification on-the- job training and testing.
+ Assists in identifying manufacturing issues by working withengineering to determine root cause and implementcorrectiveand preventative action.
+ Learns process to disposition non-conforming material byutilising quality tools and by developing knowledge of manufacturing practices andprocedures.
+ Helps to develop and implement process improvements byassisting engineering in researching and validating changes in processes/equipmentandtestmethodstoimproveyieldand/orreduce cycle time per established procedures.
+ Assists engineering in supporting process development duringnewproductintroductionbyprovidinginputtotraceabilityandinspectionrequirements,providinginputforstatisticalprocess control criteria, developing manufacturing instructions, and creating training sheets and certifications.
+ Assists engineering with qualification and validation studies andreports by collecting, compiling, meassuring, organising andrecording data, and by writing procedures. May keeplab notebook.
**EDUCATION & COMPETENCIES**
+ National Framework of Qualifications (NFQ) level 6 qualification in a relevant discipline. 2+ years of related work experience, or an equivalentcombination of education and work experience.
+ Applies broad knowledge of general technical concepts and practices and a general understanding of product or systems fundamentals. Utilises increased knowledge of numerical and statistical data and computer software programs to resolve nonroutine/moderately complex problems. Will perform this job in aquality system environment. Failure to adequately perform taskscan result in noncompliance with governmental regulations.
+ Performs non-routine to moderately complextechnical assignments using standard methods and sequences.Performs set-up, testing, repair, inspection, and/or maintenanceof al I area-specific equipment, materials, systems, and/orproduct. Makes adjustments, modifications, and replacementsas directed. Assignments require broad judgment introubleshooting proven processes as well as the ability to suggestalternatives.
+ Regularly presents findings to cross-functional teams and begins to win support for ideas. Can adequately write procedures and product disposition documentation that may be presented to external auditing bodies.
+ Mentors new team members. Ensures open communication within group and across shift and relevant functions to resolve technical issues and promote learning.
+ Plans, organises, and prioritises own daily work routine to meet established schedule.
+ Solves a variety of problems of limited to moderate scope and complexity requiring basic interpretation of defined procedures and practices. Maintains confidentiality in handling sensitive information or documents.
+ General supervision. Receives general instruction on routine work and detailed instruction on new assignments.
**REFER TO THE SITE SAFETY STATEMENT (SHE038447) FOR YOUR SAFETY, HEALTH AND WELFARE AT WORK RESPONSIBILITIES**
**Abbott Ireland is an Equal Opportunities Employer**
+ Connect with us at , on LinkedIn at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Ireland Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Our broad line of vascular devices-which includes vessel closure, endovascular and coronary technologies-are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
**PURPOSE OF THE JOB**
Provides technical assistance to engineering to support
manufacturing efforts by implementing corrective and preventative actions. Assists engineers in developing methods and procedures to control or improve manufacturing processes.
**MAJOR RESPONSIBILITIES**
+ Assists engineering in providing manufacturing support bylearning to analyse data and identify manufacturing issues and trends. May also train operators on basic processes and engineering changes, and perform operator certification on-the- job training and testing.
+ Assists in identifying manufacturing issues by working withengineering to determine root cause and implementcorrectiveand preventative action.
+ Learns process to disposition non-conforming material byutilising quality tools and by developing knowledge of manufacturing practices andprocedures.
+ Helps to develop and implement process improvements byassisting engineering in researching and validating changes in processes/equipmentandtestmethodstoimproveyieldand/orreduce cycle time per established procedures.
+ Assists engineering in supporting process development duringnewproductintroductionbyprovidinginputtotraceabilityandinspectionrequirements,providinginputforstatisticalprocess control criteria, developing manufacturing instructions, and creating training sheets and certifications.
+ Assists engineering with qualification and validation studies andreports by collecting, compiling, meassuring, organising andrecording data, and by writing procedures. May keeplab notebook.
**EDUCATION & COMPETENCIES**
+ National Framework of Qualifications (NFQ) level 6 qualification in a relevant discipline. 2+ years of related work experience, or an equivalentcombination of education and work experience.
+ Applies broad knowledge of general technical concepts and practices and a general understanding of product or systems fundamentals. Utilises increased knowledge of numerical and statistical data and computer software programs to resolve nonroutine/moderately complex problems. Will perform this job in aquality system environment. Failure to adequately perform taskscan result in noncompliance with governmental regulations.
+ Performs non-routine to moderately complextechnical assignments using standard methods and sequences.Performs set-up, testing, repair, inspection, and/or maintenanceof al I area-specific equipment, materials, systems, and/orproduct. Makes adjustments, modifications, and replacementsas directed. Assignments require broad judgment introubleshooting proven processes as well as the ability to suggestalternatives.
+ Regularly presents findings to cross-functional teams and begins to win support for ideas. Can adequately write procedures and product disposition documentation that may be presented to external auditing bodies.
+ Mentors new team members. Ensures open communication within group and across shift and relevant functions to resolve technical issues and promote learning.
+ Plans, organises, and prioritises own daily work routine to meet established schedule.
+ Solves a variety of problems of limited to moderate scope and complexity requiring basic interpretation of defined procedures and practices. Maintains confidentiality in handling sensitive information or documents.
+ General supervision. Receives general instruction on routine work and detailed instruction on new assignments.
**REFER TO THE SITE SAFETY STATEMENT (SHE038447) FOR YOUR SAFETY, HEALTH AND WELFARE AT WORK RESPONSIBILITIES**
**Abbott Ireland is an Equal Opportunities Employer**
+ Connect with us at , on LinkedIn at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.
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6
Quality Assurance Engineer, Senior
Clonmel, Munster
Abbott
Posted 20 days ago
Job Viewed
Job Description
**Abbott in Ireland**
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Ireland Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Our broad line of vascular devices-which includes vessel closure, endovascular and coronary technologies-are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
**PURPOSE OF THE JOB**
Provide Process/Quality Engineering support to manufacturing and projects helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. Will be the liaison to cross function departments (for example Research and Development, Operations and other Quality Functions). Must be able to analyze data and assist in interpreting the data. Develop and implement investigation process improvements.
**MAJOR RESPONSIBILITIES**
+ Responsible for compliance with applicable corporate and divisional policies and procedures. Estimates project levels of effort and resource requirements by using standard estimating techniques and tools, and by working with appropriate staff to understand scope of effort.
+ Prepares project plans, schedules and budgets by using project management tools such as Microsoft Project and by working with appropriate staff to understand tasks necessary to complete project.
+ Directs project execution by assigning tasks, tracking project schedules, identifying risks, and developing and executing contingency plans.
+ Communicates project status by preparing standard status reports, and by participating in departmental and customer project status update meetings.
+ Resolves project issues by working with team members, project customers, and others as appropriate.
+ Translates business strategy into meaningful objectives and day-to-day activities required to accomplish them.
+ Identifies and controls manufacturing process defects (scrap, nonconforming material, customer complaints) by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying and bounding data to support implementation of complex and documenting release criteria.
+ Develops product quality plans, documents and systems by creating product specifications, quality specifications and quality plans in conjunction with other product development team members. May be responsible for creating risk analyses and Failure Mode Effect Analysis (FMEA).
**EDUCATION & COMPETENCIES**
+ National Framework of Qualifications level 7 qualification in a relevant discipline and 4+years of related work experience, or an equivalent combination of education and work experience.
+ Wide application of technical principles, practices and procedures. Strong understanding of business unit function and cross group dependencies/relationships. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Has a sound knowledge of various technical alternatives and their impact.
+ Establishes and cultivates an extensive network of support to facilitate completion of assignments. Participates in the development of less experienced staff by setting an example, providing guidance and work direction, and offering counsel. May lead a project team. Participates in determining goals and objectives for projects. Influences middle management on technical or business solutions. May interact with vendors.
+ Plans and organises non-routine tasks with approval. Initiates or maintains work schedule. Establishes priorities of work assignments. (Decision Making/Impact) Exercises judgment in selecting innovative, practical methods to achieve problem resolution. Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources.
+ Works under only general direction. Independently determines and develops approach to solutions. Work is reviewed upon completion for adequacy in meeting objectives.
+ Will provide work direction and guidance to exempt and/or skilled nonexempt levels of employees will be asked to evaluate performance of and assist in career development planning for subordinates.
**REFER TO THE SITE SAFETY STAT** **E** **MENT (SHE038447) FOR YOUR SA** **F** **ETY, HEALTH AND WELFARE AT WORK RESPONSIBILITIES**
**Abbott Ireland is an Equal Opportunities Employer**
Connect with us at , on LinkedIn at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Ireland Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Our broad line of vascular devices-which includes vessel closure, endovascular and coronary technologies-are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
**PURPOSE OF THE JOB**
Provide Process/Quality Engineering support to manufacturing and projects helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. Will be the liaison to cross function departments (for example Research and Development, Operations and other Quality Functions). Must be able to analyze data and assist in interpreting the data. Develop and implement investigation process improvements.
**MAJOR RESPONSIBILITIES**
+ Responsible for compliance with applicable corporate and divisional policies and procedures. Estimates project levels of effort and resource requirements by using standard estimating techniques and tools, and by working with appropriate staff to understand scope of effort.
+ Prepares project plans, schedules and budgets by using project management tools such as Microsoft Project and by working with appropriate staff to understand tasks necessary to complete project.
+ Directs project execution by assigning tasks, tracking project schedules, identifying risks, and developing and executing contingency plans.
+ Communicates project status by preparing standard status reports, and by participating in departmental and customer project status update meetings.
+ Resolves project issues by working with team members, project customers, and others as appropriate.
+ Translates business strategy into meaningful objectives and day-to-day activities required to accomplish them.
+ Identifies and controls manufacturing process defects (scrap, nonconforming material, customer complaints) by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying and bounding data to support implementation of complex and documenting release criteria.
+ Develops product quality plans, documents and systems by creating product specifications, quality specifications and quality plans in conjunction with other product development team members. May be responsible for creating risk analyses and Failure Mode Effect Analysis (FMEA).
**EDUCATION & COMPETENCIES**
+ National Framework of Qualifications level 7 qualification in a relevant discipline and 4+years of related work experience, or an equivalent combination of education and work experience.
+ Wide application of technical principles, practices and procedures. Strong understanding of business unit function and cross group dependencies/relationships. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Has a sound knowledge of various technical alternatives and their impact.
+ Establishes and cultivates an extensive network of support to facilitate completion of assignments. Participates in the development of less experienced staff by setting an example, providing guidance and work direction, and offering counsel. May lead a project team. Participates in determining goals and objectives for projects. Influences middle management on technical or business solutions. May interact with vendors.
+ Plans and organises non-routine tasks with approval. Initiates or maintains work schedule. Establishes priorities of work assignments. (Decision Making/Impact) Exercises judgment in selecting innovative, practical methods to achieve problem resolution. Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources.
+ Works under only general direction. Independently determines and develops approach to solutions. Work is reviewed upon completion for adequacy in meeting objectives.
+ Will provide work direction and guidance to exempt and/or skilled nonexempt levels of employees will be asked to evaluate performance of and assist in career development planning for subordinates.
**REFER TO THE SITE SAFETY STAT** **E** **MENT (SHE038447) FOR YOUR SA** **F** **ETY, HEALTH AND WELFARE AT WORK RESPONSIBILITIES**
**Abbott Ireland is an Equal Opportunities Employer**
Connect with us at , on LinkedIn at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.
7
Senior Quality Assurance Specialist
Cork, Munster
Morgan McKinley
Posted 5 days ago
Job Viewed
Job Description
Senior Quality Assurance Specialist Location: Cork Industry: Pharmaceutical Employment Type: Full-Time Our client, a leading global pharmaceutical organization, is seeking a Senior Quality Assurance (QA) Specialist to join their dynamic team. This is a fantastic opportunity for an experienced QA professional to work in a high-impact, compliance-driven environment and play a pivotal role in ensuring product quality throughout the lifecycle. Key Responsibilities: Ensure full cGMP compliance in all project- and product-related activities and systems. Develop and implement quality policies, procedures, and continuous improvement initiatives. Support supplier qualification processes and collaborate closely with Procurement and external partners to ensure quality standards are met. Lead and manage all quality aspects of assigned projects and products, ensuring compliance with regulatory and internal standards. Oversee a broad range of QA-related areas such as: -Raw materials, supplier management, production processes -Specifications, change control, deviations, CAPA -Batch release, cleaning validation, audits, and customer complaints -Quality documentation, stability programs, regulatory compliance Provide quality support for the introduction of new products, including document review and approval. Ensure that all activities comply with Health, Safety, and Environmental standards. Be present on the manufacturing floor to offer real-time support and oversight. Qualifications & Experience: Bachelor's degree (or equivalent) in Pharmaceutical Sciences, Chemistry, Chemical Engineering 5 years of QA experience in a GMP-regulated pharmaceutical environment - mandatory Hands-on experience in a GMP operational setting Strong knowledge of GMP standards and regulatory requirements
This advertiser has chosen not to accept applicants from your region.
8
Quality Assurance Labelling Assistant
Ballina, Connacht
LGC Limited
Posted 5 days ago
Job Viewed
Job Description
Job Description What you'll be doing As part of our Quality Assurance team, you'll support the preparation and review of labelling documentation for diagnostic products - a vital step in ensuring accuracy and compliance. Your responsibilities will include: Reviewing and approving lot-specific product labels Populating and reviewing Instructions for Use (IFUs) with accurate technical data Maintaining and updating IFU templates to ensure consistency Entering and verifying data in our Technical Library (XML files) Processing label updates through our document control system Assisting with master labelling documents (labels, IFUs, packaging specs) Supporting validation activities for our auto-population system Uploading approved documentation to our internal and customer-facing platforms Following all SOPs and regulatory requirements Maintaining a clean, safe working environment and supporting additional team needs Qualifications What you'll bring We're looking for someone with: A Level 5 qualification (or equivalent) in Science, Engineering, Pharma or QA (desirable) Ideally 2+ years' experience in a regulated medical or diagnostics setting Familiarity with Microsoft Word and Excel; knowledge of Adobe InDesign and NiceLabel Pro is a plus A basic understanding of regulatory frameworks like FDA 21 CFR Part 820, ISO 13485, IVDR is beneficial Strong attention to detail and a proactive, organised approach to work Excellent teamwork and communication skills Additional Information What's in it for you? 25 days annual leave Health allowance and life assurance Retail discounts (local and national) Free 24/7 Employee Assistance Programme Recognition and reward schemes Ongoing career development and progression opportunities A supportive, inclusive culture rooted in our five core values: Passion | Curiosity | Integrity | Brilliance | Respect At LGC, we foster a culture of inclusion and collaboration. We believe that diverse perspectives lead to better outcomes and encourage applicants from all backgrounds to apply. We are an equal opportunity employer and offer reasonable accommodations to individuals with disabilities. If you require any adjustments throughout the recruitment process, please let us know. #lgcij To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.
This advertiser has chosen not to accept applicants from your region.
9