39 Verification Engineer jobs in Ireland

We are looking for a Design Verification Engineer to join our Dublin, Ireland Team!
A new opportunity for a Design Verification Engineer has arisen within the team at Curtiss-Wright. We are looking for experienced HW Test Engineers who can prove fitness for use of individual modules and/or entire complex instrumentation systems. The Ideal candidate must have experience including Schematic Capture, PCB Design Review, System and Module level debugging and regression testing experience, as well as fluent Python 3 for automation. This position offers tremendous opportunities for professional development as you will be facing emerging technologies in team-based environment in structured development cycles for prestigious aerospace clients.
As our Design Verification Engineer, you will design of individual tests (jigs and scripting) for testing of both analogue and digital circuits. Be a liaison with designers and/or technical management to resolve all issues arising for our Aerospace Instrumentation division.
**Location** : Dublin, Ireland
**Benefits**
Paid Time Off **I** Retirement with Employer Match **I** Health and Wellness Benefits **I** Learning and Development Opportunities **I** Competitive Pay **I** Bonus Scheme **I** Recognition **I** Employee Stock Purchase Plan ( **I** Inclusive & Supportive Culture ( Challenge:**
+ Liaising with designers to ensure Design for Manufacturing (DFM)/Design for Test (DFT) principles are observed.
+ Devising test suites that ensure coverage of all design goals as specified in datasheets, design documents and published standards.
+ Design of individual tests (jigs and scripting) for testing of both analogue and digital circuits.
+ Investigation and isolation of exceptions discovered.
+ Documentation to a high standard of all results and exceptions.
+ Liaison with designers and/or technical management to resolve all issues arising.
+ Transfer of type testing routines to final production tests as and where appropriate.
+ Approval of engineering documentation including schematics, bills of material, production assembly instructions etc.
+ Contribution to and approval of datasheets.
+ Adherence to and/or contribution to the development of AS9100 approved departmental procedures and work instructions.
+ Maintaining an awareness of current state of the art and competing technologies in the market.
+ Liaising with program managers, customer support teams and external bodies on product certification.
**What You Bring:**
+ Qualified to at least primary degree level or equivalent.
+ 3+ years of experience in a hardware verification or hardware development role (5+ years preferred).
+ Extensive knowledge of both analogue and digital electronics.
+ Hands on experience with Python 3, while C/C++ is minor advantage.
**About Us**
Curtiss-Wright Aerospace Instrumentation division in Dublin, Ireland provides solutions for instrumentation, telemetry, display and control, communications, recording, airborne high-speed/high-definition imaging and network-based data acquisition applications. We offer a wide range of Commercial Off The Shelf (COTS) hardware and software products for applications that require reliable, modular, programmable, miniaturized, high-performance and resilient products for commercial, defense and aerospace Flight Test applications.
Our Values ( Social and Governance
*Please note, benefits are country specific and may vary from location to location.
#LI-TS1
_No unsolicited agency submittals please. Agency partners must be invited to participate in a search by our_ **_Talent Acquisition Team ( )_** _and have signed terms in place prior to any submittal. Resumes submitted directly to any Curtiss-Wright employee or affiliate will not qualify for fee payment, and therefore become the property of Curtiss-Wright._
**Compliance Statement**
This position may require exposure to export-controlled information and subject to additional security screening. In the event information provided during the security screening reveals ineligibility to access export-controlled information, any offer of employment may be reconsidered or withdrawn.
Curtiss-Wright values diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If you require accommodation due to a disability at any time during the recruitment and/or assessment process, please contact Talent Acquisition ( ) and we will make all reasonable efforts to accommodate your request.
**Join the WRIGHT Team!**
Over 95 years of growth, Curtiss-Wright is an integrated, market-facing global diversified industrial company and remains a technology leader through this legacy of innovation. Through three well-balanced segments - Aerospace & Industrial, Defense Electronics and Naval & Power, we remain focused on advanced technologies for high performance platforms and critical applications. Diversity, commitment to excellence and dedication to the spirit of pioneering innovation continue to drive the employees of Curtiss-Wright.
**Our Values**
What makes a world-class organization? It all begins with core values that provide a strong foundation for success. Simple in theory, the values of Curtiss-Wright are reflected in every aspect of our operations. To our employees, these are more than words on a wall - we all take these values to heart in our relationships with our customers and each other.
**Leadership**
We lead based on vision and strategic direction, empowering employees to reach goals through thoughtful and decisive action.
**Customer Focus**
We are committed to achieving total quality by meeting our customers' expectations and delivering products and services in a timely fashion.
**Teamwork & Trust**
Working in a spirit of trust and collaboration, we actively encourage employees to contribute their ideas and innovations to keep our company moving forward.
**Respect for People**
We believe that people are our most valuable asset and will always do the right thing in our dealings and interactions with all employees.
**Integrity**
We will act with the highest integrity in all of our business relationships and strategic partnerships.
**What We Offer Our Employees:**
**Opportunity:** As part of the Curtiss-Wright team, you have the opportunity each day to transform the way customers do business, as well as transform your career. Our entrepreneurial environment provides you with excellent experiences that enable you to develop your skills through stretch assignments and the opportunity to work with the best talent in the industry. You will have the opportunity to contribute from day one!
**Challenging Work:** The work we do here is not only challenging, but it is meaningful to our customers, our employees and the communities in which they live and work. You are given the chance to work on some of the most advanced technology projects in the world. Now that something to be proud of!
**Collaborative Environment:** The teamwork among our exceptionally talented people enables us to deliver some of the most advanced solutions to our customers.

embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. The Verification and Validation Engineer is responsible for the execution of design verification and design validation testing in support of product lifecycle management and new product development. Responsibilities: Develops new or optimizes existing physical test methods and test fixtures to support the design verification, validation and commercialization of new medical device products and changes to existing products. Drafts engineering technical reports, test method work instructions or procedures and test method validation related documents. Leads/executes test method validation (TMV), design verification and test method transfer, in support of product design verification or validation Authors design verification protocols to satisfy product design inputs/system requirements, that satisfy applicable Quality System (QS) and regulatory requirements Manages and tracks product configurations through design verification and validation Performs hands-on and simulated testing for design verification and test method developments Conducts functional and performance testing of products to ensure that the product and its components meet the required specifications Identifies and reports out of specification results, data, and atypical/unexpected events that occur during testing activities and supports associated investigations, impact assessments and Root Cause Analysis (RCA) Educational Requirements: Minimum of Bachelor's degree in Engineering 3+ years of professional experience in the medical device, pharmaceutical or life sciences field. Relevant Experience: Applied experience in developing and qualifying test systems and methods in support of product development and launch (IQ, OQ, Measurement Systems Analysis (MSA), etc.) Experience with executing Design Verification Experience in statistical data analysis methods / tools, e.g.: Gage R&R, Hypothesis Testing Experience solving problems, provides detailed insight and constructive criticism in complex situations, and foresees problems along with potential solutions Knowledge, Skills and Abilities: Disciplined and well organized Excellent multi-tasking, analytical, communication, and prioritization skills. Ability to work independently with minimal supervision as well as in a team environment embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

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

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.

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