41 Quality Improvement jobs in Ireland

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
**Manager - Optimization and Continuous Improvement**
**Job Responsibilities:**
+ Works on more complex problems where analysis of situations or data requires in-depth evaluation of various factors, strong judgment is required in resolving problems and making recommendations (typically high impact issues that have implications across functions).
+ Supports senior leadership in creating and implementing mid-long-term plans for the Optimization and continuous improvement function.
+ Can lead projects of moderate complexity, often working cross-functionally with team members of varying levels.
+ Exceptional verbal and written communication skills. Able to create written communication that is properly structured providing clear, concise messages that draw well supported conclusions with input from the team lead; Associate Director.
+ Participates in complex projects such as the strategic review of a regions logistics infrastructure, but does not lead the project.
+ Reports project progress including the delivery of benefits.
+ Can prioritize projects to focus on delivery of benefits.
+ Assists in determining the activities to support a project's priorities within functional area.
+ Contributes to development of RFPs and participates in selection of logistics vendors.
+ Participates in the development, review and implementation of departmental SOPs and processes.
+ Ability to work within a matrix of stakeholders to deliver projects.
**KNOWLEDGE & SKILLS**
+ Experience developing and monitoring budgets and expenditures.
+ Track record of delivering projects within budget and time frame.
+ Excellent written and verbal communication.
+ Knowledge of project management tools and techniques
+ Makes cost/benefit decisions in alignment with Gilead values and expectations.
+ Ability to motivate teams and drive performance.
**Basic Qualifications:**
+ A BS/BA or MS/MA in a relevant discipline with applicable expertise
+ Proven experience in clinical or logistics coordination, demonstrating strong knowledge and practical skills in the field
**This is a hybrid role, requiring three days per week onsite and two days working remotely. Core collaboration days are Tuesday, Wednesday, and Thursday, during which onsite presence is expected.**
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

Applications are invited for a temporary post of a Continuous Improvement Lead within UCD Finance. The Finance Continuous Improvement Lead drives operational excellence in the Finance Office by analysing and optimising business processes, implementing Lean principles, and fostering a culture of continuous improvement. This position will be critical in reducing inefficiencies, improving service quality, and aligning operations with the University's strategic and operational goals. The role is to analyse current practices, identify and develop business process improvements, and implement changes in workflows to drive continuous performance. 95 Administrative Officer IA_2010 Salary Scale: €70,611 - €2,512 per annum Appointment will be made on scale and in accordance with the Department of Finance guidelines Closing date: 12:00 noon (local Irish time) on 01 September 2025 Applications must be submitted by the closing date and time specified. Any applications which are still in progress at the closing time of 12:00 noon (Local Irish Time) on the specified closing date will be cancelled automatically by the system. UCD are unable to accept late applications. UCD do not require assistance from Recruitment Agencies. Any CV's submitted by Recruitment Agencies will be returned. Tugtar cuireadh d'iarratais ar post sealadach Ceannasa Feabhschin Leannach laistigh de Ceannasa Feabhschin Leannach Tiomineann an Ceannasa Feabhschin Leannach Airgeadais srmhaitheas oibrochtil san Oifig Airgeadais tr anails a dhéanamh ar phrisis ghn agus iad a bharrfheabhs, prionsabail Lean a chur i bhfeidhm, agus cultr feabhschin leannaigh a choth. Beidh an post seo rthbhachtach chun neamhéifeachtlachta a laghd, cilocht seirbhse a fheabhs, agus oibrochta a ailni le spriocanna straitéiseacha agus oibrochtlana hOllscoile. Is é an rl n anails a dhéanamh ar chleachtais reatha, feabhsuithe ar phrisis ghn a aithint agus a fhorbairt, agus athruithe ar shreafa oibre a chur i bhfeidhm chun feidhmocht leannach a thiomint. 95 Oifigeach Riarachin 1a_2010: €70,6 - ,512 in aghaidh na bliana Déanfar an ceapachn ar scla agus de réir threoirlnte na Roinne Airgeadais Dta dnta: 12:00 uair (am itiil na hireann) ar 01.09.2025 N mr iarratas a bheith istigh faoin am agus dta at sonraithe. Déanfar aon iarratas at fs ar sil ag an am dnta 12:00 uair (Am itiil na hireann) ar an dta dnta sonraithe a scriosadh go huathoibroch ag an gcras. N féidir le UCD glacadh le hiarratais dhéanacha. Nl cnamh ag teastil UCD Ghnomhaireachta Earcaochta. Seolfar ar ais aon CV a chuir na Gnomhaireachta Earcaochta isteach. 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.

Job title:Quality Assurance Associate Location:Bishopstown, Cork. Benefits:Excellent salary, 10% bonus, hybrid working, healthcare and pension. Company: My client, spun out from Munster Technological University (formerly Cork Institute of Technology) in 2015, develops innovative ENT (Ear, Nose, and Throat) medical devices that simplify surgical procedures by enabling treatments to be conducted safely outside the operating roomtypically with just topical anesthesia. Role: You will be responsible for assisting in the maintenance of the Quality Management System (QMS), assist with the management of internal processes and external vendors to ensure product quality. This involves managing supplier relationships, participating in audits, resolving quality issues, driving continuous improvement initiatives and collaborate with various teams to maintain quality across the supply chain. The person in this position must have a working knowledge of medical device regulatory requirements and standard practices in the medical device industry. Job Requirements: Maintaining the effectiveness of the QMS and making continuous improvements to it. Managing day-to-day QA activities including frequent interface with contract manufacturers, QA consultants and testing contractors as well as handling multiple projects related to product and compliance enhancements. Responsible for assisting in notified body audits and internal audits. Maintain and coordinate quality system schedules, including: Supplier and internal audits; management review and documentation updates. Support the wider team to ensure product manufacture and testing meets the requirements. Building and maintaining strong relationships with suppliers, monitoring their performance, and conducting audits to ensure compliance with quality standards. Investigating, analysing, and resolving any product quality problems, including root cause analysis and implementing corrective and preventive actions. Ensuring that incoming materials meet the required specifications and working with the engineering team to address any quality concerns. Maintain the day-to-day activities of Post Market Surveillance, including, but not limited to: coordinating investigations between complainants and contract manufacturing sites follow up on corrective actions, when required Support with Significant Changes and Notified Body interactions. Carry out other quality related duties as required, inclusive of updates to procedures, forms, processes and periodic reviews. Education Bachelors degree in engineering or science. Quality certification in ISO 13485 a must. A minimum of 4 years of experience in a medical device QA position(s) role within a medical device organisation. Thorough understanding and knowledge of ISO 13485 and ISO 14971, EU MDR and 21 CFR Part 820. Desirable to have lead auditor certification and/or Regulatory certifications. Proven track record with the ability to successfully manage projects to deadlines. Good Documentation Practice experience. Report & Technical Writing experience. Project Management experience. Strong ability to manage critical projects as part of an interdisciplinary team. Excellent problem solving and communication skills. Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on OR Benefits: Healthcare + Annual Bonus + Pension

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

Build the future of financial markets. Build yours. Ready to make a real impact in the financial industry? At Deutsche Brse Group, we'll empower you to grow your career in a supportive and inclusive environment. With our unique business model, driven by 15,000 colleagues around the globe, we actively shape the future of financial markets. Join our One Global Team! Who we are Deutsche Brse Group is one of the world's leading exchange organisations and an innovative market infrastructure provider. With our products and services, we ensure that capital markets are fair, transparent, reliable, and stable. Together, we develop state-of-the-art IT solutions and offer our IT systems all over the world. Within the Deutsche Brse Group, Clearstream is an international central securities depository (ICSD). It provides post-trade infrastructure and securities services for the international market and 59 domestic markets worldwide, with customers in 110 countries. Cork Your career at Deutsche Brse Group Your area of work The Quality Control Officer is responsible for ensuring the accuracy, consistency, and completeness of regulatory reporting outputs across KIIDs, PRIIPs and ESG domains. This role supports the delivery of high-quality reports by performing detailed quality checks, identifying discrepancies, and driving continuous improvement in data validation and reporting processes. Your responsibilities Perform detailed quality control checks on KIIDs, PRIIPs and ESG reports prior to client delivery, ensuring alignment with regulatory standards and internal quality benchmarks. Identify and document errors, inconsistencies, and missing narratives across reporting outputs. Collaborate with Regulatory Reporting Agents to validate data sources and ensure accurate interpretation of regulatory requirements. Monitor and report on recurring quality issues, contributing to root cause analysis and recommending corrective actions. Support the enhancement of validation tools and processes to reduce false positives and improve reporting accuracy. Maintain quality logs and KPIs to track performance and support post-production reviews. Liaise with internal teams to ensure timely resolution of quality issues and escalate critical findings to management. Assist in the development and implementation of quality assurance procedures and best practices. Participate in assigned training and stay updated on regulatory changes impacting reporting standards. Act and work in compliance with all internal rules and policies. Your profile A minimum of 3 years of post-graduate education, preferably in Finance, Data Management, or a related field At least 2 years of experience in a quality assurance, data validation, or regulatory reporting role Understanding of ESG, KIID, and PRIIPs reporting standards and regulatory frameworks Proficiency in English; additional languages are an asset Advanced Microsoft Excel skills and familiarity with data validation tools Excellent attention to detail and analytical skills Strong communication and interpersonal skills Proactive, solution-oriented mindset with a collaborative approach Ability to work independently and manage multiple priorities

Your new company Our client is seeking a QA Analyst to support Ireland and UK operations, ensuring compliance with standards and regulations, and maintaining audit integrity, supplier quality, and operational controls. Your new role Audit Program Support Plan, execute, and follow up on internal, external, and corporate audits. Maintain audit documentation and ensure timely resolution of findings. Supplier Quality Management Conduct supplier audits and evaluations. What you'll need to succeed Proven experience in quality assurance within medical devices or healthcare technology. In-depth knowledge of ISO ,EU MDR, EU MDD, and UK MDR. Certified Lead Auditor for ISO 13485 or equivalent. Familiarity with supplier management protocols and regulatory compliance. Strong documentation and audit skills. Ability to work independently and collaboratively across regions. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career. Hays Ireland is a trading division of Hays Specialist Recruitment (Ireland) Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be Benefits: 12-month contract

Quality Assurance Technician We are currently seeking two dedicated Quality Assurance Technician's to join a dynamic and growing team within the food manufacturing sector. This role is key to ensuring products meet the highest standards of quality, safety, and compliance, while driving continuous improvement initiatives. If you're passionate about quality, enjoy problem-solving, and thrive in a fast-paced production environment, this could be the perfect opportunity for you. Key Responsibilities Monitor production performance against KPIs relating to output, waste, and cost. Execute the production plan, ensuring adherence to running order and volumes. Train and mentor new team members and agency staff within the department. Promote and implement good housekeeping practices, leading by example. Enforce Health & Safety, Food Safety, and Hygiene standards at all times. Verify products meet established quality specifications and customer requirements. Assess incoming raw materials against quality standards. Collect and prepare samples for laboratory testing. Carry out regular in-process checks to ensure consistent product quality. Maintain accurate quality control records and documentation. Ensure compliance with food safety regulations, including HACCP standards. Skills & Experience Experience collaborating effectively with operations, technical, and hygiene teams. Proactive, solutions-focused mindset with a willingness to take ownership. Strong motivation to uphold high standards and inspire others to do the same. Competent in Microsoft Word and Excel. Flexible approach to working hours to support business needs. Ability to work independently as well as part of a team. Strong communication and problem-solving skills. Driven to meet and exceed targets. This is a fantastic opportunity for someone with a passion for quality assurance to make a real impact in a forward-thinking manufacturing environment.

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,

**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