56 Qa Consulting jobs in Ireland

Software Quality Assurance Engineer Location: Galway (Hybrid) Type: Contract Our client is looking to hire Software Quality Assurance Engineer. Working inside a scrum team alongside software engineers and systems analysts, you will shape and deliver the QA automation approach for applications to enable fast, reliable delivery of customer features supporting Institutional clients. You will help design, build and maintain secure, high-performance, scalable systems that support the Institutional business. Your experience: Minimum 5+ years experience in software quality engineering. Hands-on experience building test automation using frameworks/tools such as Cucumber, Karate, Selenium, Test NG, Soap UI. Practical knowledge of continuous integration practices and automated deployment tooling. Proficient in Java or another equivalent object-oriented programming language. Solid SQL skills and a good understanding of databases. Familiarity with one or more of: Spring / Spring Boot, Angular (or other Java Script/Type Script frameworks), and RESTful services. Experience with AWS or similar cloud platforms. Comfortable working within Agile ways of working and attending Agile ceremonies. Excellent oral and written communication skills. Your responsibilities: Help define acceptance criteria and translate them into release testing needs by collaborating with engineering and business stakeholders. Architect, build and run functional and regression test cases and suites. Reproduce, diagnose and isolate defects and confirm fixes. Analyse and present test outcomes, contributing to project tracking and assessing product release readiness. Contribute to the teams QA automation strategy to accelerate delivery of priority features. If you are interested in learning more about this opportunity, please drop me a message, forward your CV using the apply button or reach out to me directly via #LI-CF3 Skills: Cucumber Karate Selenium Test NG Soap UI Spring Boot Angular

Software Quality Assurance Engineer Location: Galway (Hybrid) Type: Contract Our client is looking to hire Software Quality Assurance Engineer.

Working inside a scrum team alongside software engineers and systems analysts, you will shape and deliver the QA automation approach for applications to enable fast, reliable delivery of customer features supporting Institutional clients.

You will help design, build and maintain secure, high-performance, scalable systems that support the Institutional business.

Your experience: Minimum 5+ years experience in software quality engineering.

Hands-on experience building test automation using frameworks/tools such as Cucumber, Karate, Selenium, Test NG, Soap UI.

Practical knowledge of continuous integration practices and automated deployment tooling.

Proficient in Java or another equivalent object-oriented programming language.

Solid SQL skills and a good understanding of databases.

Familiarity with one or more of: Spring / Spring Boot, Angular (or other Java Script/Type Script frameworks), and RESTful services.

Experience with AWS or similar cloud platforms.

Comfortable working within Agile ways of working and attending Agile ceremonies.

Excellent oral and written communication skills.

Your responsibilities: Help define acceptance criteria and translate them into release testing needs by collaborating with engineering and business stakeholders.

Architect, build and run functional and regression test cases and suites.

Reproduce, diagnose and isolate defects and confirm fixes.

Analyse and present test outcomes, contributing to project tracking and assessing product release readiness.

Contribute to the teams QA automation strategy to accelerate delivery of priority features.

If you are interested in learning more about this opportunity, please drop me a message, forward your CV using the apply button or reach out to me directly via #LI-CF3 Skills: Cucumber Karate Selenium Test NG Soap UI Spring Boot Angular

It all started in sunny San Diego, California in 2004 when a visionary engineer, Fred Luddy, saw the potential to transform how we work. Fast forward to today - ServiceNow stands as a global market leader, bringing innovative AI-enhanced technology to over 8,100 customers, including 85% of the Fortune 500®. Our intelligent cloud-based platform seamlessly connects people, systems, and processes to empower organizations to find smarter, faster, and better ways to work. But this is just the beginning of our journey. Join us as we pursue our purpose to make the world work better for everyone.
**What you get to do in this role:** **  **
+ Maintain existing automation test frameworks
+ Collect and report quality metrics from test execution
+ Work with developers to design specific testing strategies for features being developed and automate them
+ Create comprehensive test plans; execute and automate them
+ Support engineering organizations in troubleshooting or addressing issues with applications and dev/test environments
**To be successful in this role you have:**
+ Experience in leveraging or critically thinking about how to integrate AI into work processes, decision-making, or problem-solving. This may include using AI-powered tools, automating workflows, analyzing AI-driven insights, or exploring AI's potential impact on the function or industry.
+ 5+ years of experience with quality assurance and Java programming with Selenium, JUnit and TestNG
+ Fluency with scripting in JavaScript. Experience with Eclipse, Jenkin, Maven, and Git
+ Understanding of testing techniques (e.g. performance, unit, integration, automated), their strengths and weakness, and ability to use them to best effect
+ Ability to use tools (such as IDE, debugger, build tools, source control, ServiceNow instances, profilers, system administration/Unix tools) to assist with daily tasks
+ Experience driving cross-team technical discussions with an understanding of SDLC concepts
**Work Personas**
We approach our distributed world of work with flexibility and trust. Work personas (flexible, remote, or required in office) are categories that are assigned to ServiceNow employees depending on the nature of their work and their assigned work location. Learn more here ( . To determine eligibility for a work persona, ServiceNow may confirm the distance between your primary residence and the closest ServiceNow office using a third-party service.
**Equal Opportunity Employer**
ServiceNow is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex, sexual orientation, national origin or nationality, ancestry, age, disability, gender identity or expression, marital status, veteran status, or any other category protected by law. In addition, all qualified applicants with arrest or conviction records will be considered for employment in accordance with legal requirements.
**Accommodations**
We strive to create an accessible and inclusive experience for all candidates. If you require a reasonable accommodation to complete any part of the application process, or are unable to use this online application and need an alternative method to apply, please contact for assistance.
**Export Control Regulations**
For positions requiring access to controlled technology subject to export control regulations, including the U.S. Export Administration Regulations (EAR), ServiceNow may be required to obtain export control approval from government authorities for certain individuals. All employment is contingent upon ServiceNow obtaining any export license or other approval that may be required by relevant export control authorities.
From Fortune. ©2025 Fortune Media IP Limited. All rights reserved. Used under license.

It all started in sunny San Diego, California in 2004 when a visionary engineer, Fred Luddy, saw the potential to transform how we work. Fast forward to today - ServiceNow stands as a global market leader, bringing innovative AI-enhanced technology to over 8,100 customers, including 85% of the Fortune 500®. Our intelligent cloud-based platform seamlessly connects people, systems, and processes to empower organizations to find smarter, faster, and better ways to work. But this is just the beginning of our journey. Join us as we pursue our purpose to make the world work better for everyone.
**What you get to do in this role:** **  **
+ Maintain existing automation test frameworks
+ Collect and report quality metrics from test execution
+ Work with developers to design specific testing strategies for features being developed and automate them
+ Create comprehensive test plans; execute and automate them
+ Support engineering organizations in troubleshooting or addressing issues with applications and dev/test environments
**To be successful in this role you have:**
+ Experience in leveraging or critically thinking about how to integrate AI into work processes, decision-making, or problem-solving. This may include using AI-powered tools, automating workflows, analyzing AI-driven insights, or exploring AI's potential impact on the function or industry.
+ 5+ years of experience with quality assurance and Java programming with Selenium, JUnit and TestNG
+ Fluency with scripting in JavaScript. Experience with Eclipse, Jenkin, Maven, and Git
+ Understanding of testing techniques (e.g. performance, unit, integration, automated), their strengths and weakness, and ability to use them to best effect
+ Ability to use tools (such as IDE, debugger, build tools, source control, ServiceNow instances, profilers, system administration/Unix tools) to assist with daily tasks
+ Experience driving cross-team technical discussions with an understanding of SDLC concepts
**Work Personas**
We approach our distributed world of work with flexibility and trust. Work personas (flexible, remote, or required in office) are categories that are assigned to ServiceNow employees depending on the nature of their work and their assigned work location. Learn more here ( . To determine eligibility for a work persona, ServiceNow may confirm the distance between your primary residence and the closest ServiceNow office using a third-party service.
**Equal Opportunity Employer**
ServiceNow is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex, sexual orientation, national origin or nationality, ancestry, age, disability, gender identity or expression, marital status, veteran status, or any other category protected by law. In addition, all qualified applicants with arrest or conviction records will be considered for employment in accordance with legal requirements.
**Accommodations**
We strive to create an accessible and inclusive experience for all candidates. If you require a reasonable accommodation to complete any part of the application process, or are unable to use this online application and need an alternative method to apply, please contact for assistance.
**Export Control Regulations**
For positions requiring access to controlled technology subject to export control regulations, including the U.S. Export Administration Regulations (EAR), ServiceNow may be required to obtain export control approval from government authorities for certain individuals. All employment is contingent upon ServiceNow obtaining any export license or other approval that may be required by relevant export control authorities.
From Fortune. ©2025 Fortune Media IP Limited. All rights reserved. Used under license.

**Job Description Summary**
The Senior Software Quality Engineer is accountable for supporting the Research Centre Ireland (RCI) site, RCI Project teams and/or other projects intended to enhance RCI's operational effectiveness, including the initial creation of a Quality Management System for the RCI site. The Sr. Quality Engineer focuses on the creation of quality processes and procedures at the RCI site which support design control, process control & validation, supplier management and technology transfer based on industry and BD best practices.
**Job Description**
**We are the makers of possible**
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
**Why join us?**
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a **maker of possible** with us!
**Our vision for** **Peripheral Intervention** **at BD**
Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, and end-stage renal disease and maintenance.
**About the role**
The Senior Software Quality Engineer plays a pivotal role as an emerging Subject Matter Expert within cross-functional project teams, particularly in areas such as new product development, manufacturing transfer, and special initiatives. This role ensures that software-related deliverables meet customer expectations and comply with a wide range of regulatory standards, including 21CFR820, 21CFR11, ISO 13485, ISO 14971, IEC 62304, IVDD 98/79/EEC, and EU MDR 2017/745. The engineer is responsible for guiding computer system validation efforts and assessing compliance with electronic records regulations, while also overseeing key quality processes such as design planning, risk management, design reviews, and change control for both application and embedded software.
In addition to regulatory and project responsibilities, the Senior Software Quality Engineer reviews and approves critical documentation, including product drawings and verification/validation protocols. They apply statistical tools to analyse data, identify root causes, and drive effective problem resolution. Their expertise ensures that software products are developed and released with robust quality assurance, aligning with both internal standards and external regulatory requirements. This role is essential for maintaining product integrity and supporting continuous improvement across software development and quality functions.
**Main responsibilities will include:**
+ Develop, enhance and maintain strategies and plans to improve the overall quality of software, including test coverage and system performance.
+ Provides strategic and tactical support of the Quality Engineering Function, based on an understanding of 21 CFR Part 820 and ISO Requirements.
+ Owns and facilitates the Design Review and Functional Review Process for software products.
+ Collaborates with Manufacturing and R&D to support software products, driving design improvements and monitoring measurable enhancements. Routinely interacts with multifunctional groups.
+ Ensures BD PI Systems divisional, departmental policies, procedures, practices, and facilities are in compliance with all applicable regulatory guidelines.
+ Represent the Quality Function for New Product Development Core Teams and/or Technology Transfer Core Team
+ Plays a key role as a core team member in software development projects, handling various tasks such as requirements, SW development planning, risk management, V&V, and other work.
+ Remediates software-related audit findings and CAPAs.
**About you**
+ Bachelor's degree in Electrical, Mechanical, Software or Biomedical Engineering or other relevant technical area with 6 to 7 years of experience, where 4 of those years are progressive experience in software development or lifecycle management. Or MS/MBA with 7 years of experience, where 5 of those years are progressive experience in software development or lifecycle management.
+ Ability and skill to effectively manage multiple tasks and lead execution of change management plans
+ Ability and skill to handle the Quality function for design projects, reliability concepts for complex systems, validation planning and statistical sampling, Six Sigma root cause analysis tools and project management techniques
+ Ability to effectively write communications that ensure clarity, accuracy and consideration of the audience
+ Ability to speak with clarity and express points of view in a variety of settings: one-on-one interactions, group meetings, and formal presentations
+ Ability to listen to others, including associates, managers, peers and customers, when making decisions and solving problems
+ Ability and skill to analyse using systematic analysis tools that include root cause, failure analysis and risk assessment to gather critical information and diagnose
+ Ability to drive for results and effectively work through conflicts in working teams by facilitating conflict resolution
+ Working knowledge and understanding of the Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO).
**Click on apply if this sounds like you!**
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to 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, and other legally-protected characteristics.
**To learn more about BD visit:** ** Skills
Optional Skills
.
**Primary Work Location**
IRL Limerick - Castletroy
**Additional Locations**
**Work Shift**
At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You ( .
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed.
The salary or hourly rate offered to a successful candidate is determined by their experience, education, and skills, as well as the labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location.
**Salary Range Information**
54,800.00 - 93,200.00 EUR Annual
Becton, Dickinson and Company 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.

Job Description Summary The Senior Software Quality Engineer is accountable for supporting the Research Centre Ireland (RCI) site, RCI Project teams and/or other projects intended to enhance RCI's operational effectiveness, including the initial creation of a Quality Management System for the RCI site. The Sr. Quality Engineer focuses on the creation of quality processes and procedures at the RCI site which support design control, process control & validation, supplier management and technology transfer based on industry and BD best practices. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. Why join us? A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place. Become a maker of possible with us! Our vision for Peripheral Intervention at BD Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, and end-stage renal disease and maintenance. About the role The Senior Software Quality Engineer plays a pivotal role as an emerging Subject Matter Expert within cross-functional project teams, particularly in areas such as new product development, manufacturing transfer, and special initiatives. This role ensures that software-related deliverables meet customer expectations and comply with a wide range of regulatory standards, including 21CFR820, 21CFR11, ISO 13485, ISO 14971, IEC 62304, IVDD 98/79/EEC, and EU MDR 2017/745. The engineer is responsible for guiding computer system validation efforts and assessing compliance with electronic records regulations, while also overseeing key quality processes such as design planning, risk management, design reviews, and change control for both application and embedded software. In addition to regulatory and project responsibilities, the Senior Software Quality Engineer reviews and approves critical documentation, including product drawings and verification/validation protocols. They apply statistical tools to analyse data, identify root causes, and drive effective problem resolution. Their expertise ensures that software products are developed and released with robust quality assurance, aligning with both internal standards and external regulatory requirements. This role is essential for maintaining product integrity and supporting continuous improvement across software development and quality functions. Main responsibilities will include: Develop, enhance and maintain strategies and plans to improve the overall quality of software, including test coverage and system performance. Provides strategic and tactical support of the Quality Engineering Function, based on an understanding of 21 CFR Part 820 and ISO Requirements. Owns and facilitates the Design Review and Functional Review Process for software products. Collaborates with Manufacturing and R&D to support software products, driving design improvements and monitoring measurable enhancements. Routinely interacts with multifunctional groups. Ensures BD PI Systems divisional, departmental policies, procedures, practices, and facilities are in compliance with all applicable regulatory guidelines. Represent the Quality Function for New Product Development Core Teams and/or Technology Transfer Core Team Plays a key role as a core team member in software development projects, handling various tasks such as requirements, SW development planning, risk management, V&V, and other work. Remediates software-related audit findings and CAPAs. About you Bachelor's degree in Electrical, Mechanical, Software or Biomedical Engineering or other relevant technical area with 6 to 7 years of experience, where 4 of those years are progressive experience in software development or lifecycle management. Or MS/MBA with 7 years of experience, where 5 of those years are progressive experience in software development or lifecycle management. Ability and skill to effectively manage multiple tasks and lead execution of change management plans Ability and skill to handle the Quality function for design projects, reliability concepts for complex systems, validation planning and statistical sampling, Six Sigma root cause analysis tools and project management techniques Ability to effectively write communications that ensure clarity, accuracy and consideration of the audience Ability to speak with clarity and express points of view in a variety of settings: one-on-one interactions, group meetings, and formal presentations Ability to listen to others, including associates, managers, peers and customers, when making decisions and solving problems Ability and skill to analyse using systematic analysis tools that include root cause, failure analysis and risk assessment to gather critical information and diagnose Ability to drive for results and effectively work through conflicts in working teams by facilitating conflict resolution Working knowledge and understanding of the Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO). Click on apply if this sounds like you! At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to 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, and other legally-protected characteristics.

Job Description Summary The Senior Software Quality Engineer is accountable for supporting the Research Centre Ireland (RCI) site, RCI Project teams and/or other projects intended to enhance RCI's operational effectiveness, including the initial creation of a Quality Management System for the RCI site.

The Sr. Quality Engineer focuses on the creation of quality processes and procedures at the RCI site which support design control, process control & validation, supplier management and technology transfer based on industry and BD best practices.

Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world.

Advancing the world of health is our Purpose, and it's no small feat.

It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Why join us? A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture.

You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do.

We welcome people with the imagination and drive to help us reinvent the future of health.

At BD, you'll discover a culture in which you can learn, grow and thrive.

And find satisfaction in doing your part to make the world a better place.

Become a maker of possible with us! Our vision for Peripheral Intervention at BD Our Peripheral Intervention (PI) business unit offers a comprehensive range of medical products, devices and services for the treatment of peripheral arterial and venous disease, cancer detection, and end-stage renal disease and maintenance.

About the role The Senior Software Quality Engineer plays a pivotal role as an emerging Subject Matter Expert within cross-functional project teams, particularly in areas such as new product development, manufacturing transfer, and special initiatives.

This role ensures that software-related deliverables meet customer expectations and comply with a wide range of regulatory standards, including 21 CFR820, 21 CFR11, ISO 13485, ISO 14971, IEC 62304, IVDD 98/79/EEC, and EU MDR 2017/745.

The engineer is responsible for guiding computer system validation efforts and assessing compliance with electronic records regulations, while also overseeing key quality processes such as design planning, risk management, design reviews, and change control for both application and embedded software.

In addition to regulatory and project responsibilities, the Senior Software Quality Engineer reviews and approves critical documentation, including product drawings and verification/validation protocols.

They apply statistical tools to analyse data, identify root causes, and drive effective problem resolution.

Their expertise ensures that software products are developed and released with robust quality assurance, aligning with both internal standards and external regulatory requirements.

This role is essential for maintaining product integrity and supporting continuous improvement across software development and quality functions.

Main responsibilities will include: Develop, enhance and maintain strategies and plans to improve the overall quality of software, including test coverage and system performance.

Provides strategic and tactical support of the Quality Engineering Function, based on an understanding of 21 CFR Part 820 and ISO Requirements.

Owns and facilitates the Design Review and Functional Review Process for software products.

Collaborates with Manufacturing and R&D to support software products, driving design improvements and monitoring measurable enhancements.

Routinely interacts with multifunctional groups.

Ensures BD PI Systems divisional, departmental policies, procedures, practices, and facilities are in compliance with all applicable regulatory guidelines.

Represent the Quality Function for New Product Development Core Teams and/or Technology Transfer Core Team Plays a key role as a core team member in software development projects, handling various tasks such as requirements, SW development planning, risk management, V&V, and other work.

Remediates software-related audit findings and CAPAs.

About you Bachelor's degree in Electrical, Mechanical, Software or Biomedical Engineering or other relevant technical area with 6 to 7 years of experience, where 4 of those years are progressive experience in software development or lifecycle management.

Or MS/MBA with 7 years of experience, where 5 of those years are progressive experience in software development or lifecycle management.

Ability and skill to effectively manage multiple tasks and lead execution of change management plans Ability and skill to handle the Quality function for design projects, reliability concepts for complex systems, validation planning and statistical sampling, Six Sigma root cause analysis tools and project management techniques Ability to effectively write communications that ensure clarity, accuracy and consideration of the audience Ability to speak with clarity and express points of view in a variety of settings: one-on-one interactions, group meetings, and formal presentations Ability to listen to others, including associates, managers, peers and customers, when making decisions and solving problems Ability and skill to analyse using systematic analysis tools that include root cause, failure analysis and risk assessment to gather critical information and diagnose Ability to drive for results and effectively work through conflicts in working teams by facilitating conflict resolution Working knowledge and understanding of the Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO).

Click on apply if this sounds like you! At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry.

For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance.

Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

Becton, Dickinson and Company is an Equal Opportunity Employer.

We evaluate applicants without regard to 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, and other legally-protected characteristics.

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**_Quality Assurance Student_**
Working with the Quality team to help maintain quality standards throughout the company. The brief requires knowledge of Good Manufacturing Practice, current FDA and EMEA regulations for solid oral dosage pharmaceuticals for human use and a good working knowledge of manufacturing processes and packaging processes used in the pharmaceutical industry in Bray.
**_How you will contribute_** **_:_**
+ To assist in the investigation into non-conformances, participate in root cause analysis and carry out quality review of non-conformances.
+ To assist in preparation of communication to external partners
+ Preparation and revision of cGMP documentation as required including;
+ Annual Product Reviews
+ Standard Operating Procedures
+ GMP forms
+ Product specification
+ Technical Reports and Protocols
+ Preparation of Certificate of Analysis
+ Support the site Quality Management systems including;
+ Non-Conformance and CAPA Management systems
+ Change Control system
+ Internal Auditing programs
+ GMP Training
+ Customer Complaints
+ Vendor Management program.
+ Participate in and facilitate continuous improvement projects as required
+ Control/storage of retain samples, including periodic retain inspection
+ Archiving GMP documents
In this position you will report to the **Quality Executive** **.**
**_What you bring to Takeda_** **:**
+ Participate fully in any cross functional training initiatives.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Participate in driving Quality Culture within workplace.
+ Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
+ Excellent verbal and written communication skills.
+ Be self-motivated, flexible, organized and a good team player with the ability to prioritize own work based on departmental and site requirements.
+ Experience in the pharmaceutical industry would be preferable but is not essential
**_What Takeda can offer you:_**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**_More about us:_**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**_How we will support you:_**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time

**Job title** **:** **Quality Assurance Intern**
+ Location: Waterford, Ireland
+ Start date: January 2026
+ Duration: 6-8 months
**About the job**
As a **Quality Assurance Intern** , you'll play an important role in supporting the success of our Quality Department. You'll help maintain a safe, efficient, and well-functioning aseptic filling environment working in line with Good Manfuacturing Practice (GMP). This is a hands-on opportunity to gain real-world experience while contributing to meaningful work. You'll be encouraged to engage with our Continuous Improvement programme, sharing your ideas and fresh perspective to help enhance how we fill and release from a prefilled syringe filling line.
Throughout your internship, you'll be expected to follow all regulatory and safety guidelines - protecting yourself, your colleagues, and ultimately, our patients.
Ready to grow your skills while helping shape the future of healthcare? At Sanofi, you'll be empowered to learn, ask questions, and bring your ideas to life - all while supported by inspiring mentors and collaborative teams.
**About Sanofi**
We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system - and innovative pipeline - enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.
**Main responsibilities:**
+ Working as part of the Quality Assurance team on site ensuring products are manufactured, in accordance with cGMP.
+ To ensure that all work carried out is in compliance with the required standards conforming to company, cGMPs, cGLPs, SOPs, regulatory regulations and guidelines.
+ Perform timely review of documentation / investigations / reports highlighting and assisting in the resolution of concerns commensurate with the risk.
+ Participate in the preparation and review of procedures and batch documentation.
+ Review and approval of deviation, CAPA's, quality events, change controls and tasks.
+ Acts as Quality Point person for processes providing guidance / feedback on quality issues.
+ Work with relevant departments to ensure timely closure of quality actions / findings.
+ Actively contribute to continuous improvement initiatives.
+ Conduct duties in a safe manner and report all safety issues or concerns.
**About you**
To excel in this role, you will need to:
+ Be a **2nd or 3rd year third-level student** , preferably from a **science-related discipline**
+ Communicate effectively and facilitate discussions with confidence
+ Demonstrate flexibility, drive, and a proactive, innovative mindset
+ Collaborate well with others and contribute positively to team dynamics
+ Show strong independence and self-motivation in managing tasks and learning opportunities
**Why choose us?**
+ Stretch your skills through apprenticeships, internships, graduate programs, and international experiences that grow with you.
+ Learn from inspiring mentors and collaborative teams while contributing to real projects that shape the future of healthcare.
+ Build your future with access to the latest tools, digital innovation, and continuous learning that keep you ahead of the curve.
+ Explore more with personalized development plans, short-term gigs, and internal mobility across functions and countries.
+ Grow in a purpose-driven company where your voice matters and your work helps improve millions of lives.
+ Thrive in inclusive, flexible workplaces that support your personal and professional well-being.
+ Launch your career with a company that invests in you - and empowers you to reimagine what's possible.
#LI-EUR
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (