51 Pfizer jobs in Ireland

**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 (

We are looking for a Quality Assurance Engineer to join our dynamic product team. You will play a critical role in ensuring our software meets high standards for performance, usability, and security. This includes designing and executing manual and automated test cases, tracking defects, and working closely with developers to resolve issues.
This is a hands-on role covering both manual and automated testing, with opportunities to work on backend testing, performance testing, and security testing initiatives.
Key Responsibilities
+ Develop and maintain detailed test plans, documentation, and reports using testing tools (e.g., TestRail).
+ Conduct manual testing including smoke, functional, and exploratory testing.
+ Write and maintain automated tests such as regression suites using tools like Selenium.
+ Identify, document, and track defects through to resolution.
+ Collaborate with developers, product managers, and stakeholders to ensure product quality at every stage.
+ Participate in release readiness activities, ensuring quality criteria are met before deployment.
YOU MUST HAVE
+ Proven experience in test planning, reporting, and documentation.
+ Proficiency in manual testing methodologies (smoke, functional, exploratory).
+ Experience writing automated tests (e.g., regression) with tools such as Selenium.
WE VALUE
+ Experience with backend testing tools such as Postman or curl.
+ Knowledge of penetration testing and security testing.
+ Experience in performance testing and interpreting results.
NICE TO HAVE
+ Statistical and data analysis skills.
+ Familiarity with CI/CD pipelines and integration of tests into build processes.
+ Scripting skills in Python, Bash, or similar languages.
**Our Offer**
+ The chance to work on sustainability-focused software with global impact.
+ A collaborative team environment where quality is a top priority.
+ Opportunities to expand into performance, security, and backend testing areas.
+ Competitive salary and benefits package.
We are an equal opportunity employer and value diversity at our company. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
**Join us now and be part of a global team of thinkers, innovators, dreamers, and doers who make the things that make the future!**
#TheFutureIsWhatWeMakeIt
Honeywell helps organizations solve the world's most complex challenges in automation, the future of aviation and energy transition. As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments - powered by our Honeywell Forge software - that help make the world smarter, safer and more sustainable.
Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.

Acuity Inc. (NYSE: AYI) is a market-leading industrial technology company. We use technology to solve problems in spaces, light and more things to come. Through our two business segments, Acuity Brands Lighting (ABL) and Acuity Intelligent Spaces (AIS), we design, manufacture, and bring to market products and services that make a valuable difference in people's lives.
We achieve growth through the development of innovative new products and services, including lighting, lighting controls, building management solutions, and an audio, video and control platform. We focus on customer outcomes and drive growth and productivity to increase market share and deliver superior returns. We look to aggressively deploy capital to grow the business and to enter attractive new verticals.
Our Digital Centre of Excellence in Cork, Ireland brings together the best of Acuity's technologies, serving as a hub for research and development to build software expertise, innovation and capacity. Our Digital Centre of Excellence in Cork is more than a workplace - it's a hub for innovation, collaboration, and growth. We're building a team of disruptive thinkers, data-forward engineers, and product innovators who are shaping the future of our technology.
We offer:
+ Meaningful Work: Solve real-world problems, guided by our Better.Smarter.Faster. operating system, through cutting-edge software, AI, and data solutions.
+ Growth & Development: Access to global learning experiences, mentorship, and career mobility.
+ Health & Well-Being: Comprehensive benefits and wellness programs tailored to support you.
+ Values Driven Culture: Become part of an environment where the best people come to do their best work.
+ Global Reach, Local Impact: Be part of a multinational company while contributing to Cork's vibrant tech ecosystem.
Acuity Inc. is based in Atlanta, Georgia, with operations across North America, Europe and Asia. The Company is powered by approximately 13,000 dedicated and talented associates. Visit us at . Explore opportunities in Ireland at acuityinc.ie/careers .
**Location** : Cork, Ireland (On-site)
**Job Summary**
We are seeking detail-oriented and strong Technical QA Engineers to join our team in Ireland. In this role, you will have the responsibility of ensuring the quality and reliability of software and systems through rigorous testing, automation, and process improvement. You will design, develop and execute test cases as well as collaborate across a highly matrixed team of developers, product managers and stakeholders. You will support release management and post-deployment validation, conduct functional, regression, integration and performance testing.
Successful candidates must have a strong understanding of QA methodologies, software development life cycles, and regulatory compliance standards relevant to the Irish and EU markets.
**Minimum Qualifications**
+ Bachelor's degree in Computer Science, Engineering, or related field.
+ Relevant experience in test automation tools and programming/scripting languages.
+ Preferred experience in using Co-Pilot or other AI applications.
We value diversity and are an equal opportunity employer.  All qualified applicants will be considered for employment without regards to race, color, age, gender, sexual orientation, gender identity and expression, ethnicity or national origin, disability, pregnancy, religion, covered veteran status, protected genetic information, or any other characteristic protected by law.  Please click here ( and here ( for more information.
Accommodation for Applicants with Disabilities:  As an equal opportunity employer, Acuity Inc. is committed to providing reasonable accommodations in its application process for qualified individuals with disabilities and disabled veterans. If you have difficulty using our online system due to a disability and need an accommodation, you may contact us at .  Please clearly indicate what type of accommodation you are requesting and for what requisition. 
Any unsolicited resumes sent to Acuity Inc. from a third party, such as an Agency recruiter, including unsolicited resumes sent to an Acuity Inc. mailing address, fax machine or email address, directly to Acuity Inc. employees, or to Acuity Inc. resume database will be considered Acuity Inc. property. Acuity Inc. will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Acuity Inc. will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor, but does not have the appropriate approvals to be engaged on a search.
E-Verify Participation Poster ( (

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are hiring a Quality Assurance Manager to lead our QA team at the Ballytivnan site. This role is responsible for ensuring that all products manufactured at AbbVie meet the requirements of GMP, end users, Regulatory Authorities, and AbbVie standards. The Quality Assurance Manager will oversee team performance, compliance activities, audits/inspections, and serve as a critical partner to operational functions to maintain and improve quality across the site.
Key Responsibilities:
+ Ensure products manufactured at AbbVie meet requirements of end users, Regulatory Authorities, and AbbVie.
+ Lead and manage the Quality Assurance team, providing guidance and support on quality and compliance matters.
+ Act as a site contact for regulatory and customer audits/inspections (FDA, HPRA, etc.) and prepare site teams for successful outcomes.
+ Manage CAPA (Corrective and Preventive Action) implementation, and follow-up activities.
+ Collaborate cross-functionally to resolve quality issues, improve processes, and ensure continuous compliance with cGMP and other relevant regulations.
+ Promote department goals by attracting, developing, and retaining capable QA staff.
+ Contribute to talent management and professional development of QA personnel.
+ Develop, review, and approve QA documentation as related to general QA activities.
+ Provide oversight of batch record review, deviation investigations, change controls, and product release decisions.
+ Support quality meetings and key quality metrics and trends.
+ Communicate effectively with internal and external stakeholders, including the AbbVie Quality and Compliance Group and regulatory bodies.
+ Serve as a designee for the Biologics Quality Director as required.
Qualifications
+ Bachelor's degree in science, Quality, Engineering, or related field (Master's preferred)
+ Minimum of 8 years' experience in the healthcare, pharmaceutical, or biopharmaceutical industry
+ At least 3 years' supervisory/people management experience
+ Demonstrated experience with audits and/or inspections (FDA, HPRA, etc.)
+ High level of expertise in day-to-day quality and compliance decision-making
+ In-depth knowledge of GMP requirements and regulatory frameworks
+ Strong attention to detail and commitment to compliance and quality standards
+ Ability to facilitate quality decision-making while maintaining a strong patient focus and upholding AbbVie's reputation
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

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

LSC have a great opportunity for a Senior QA Specialist to join a South Dublin-based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 7+ years of experience in construction management/engineering within the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Act as Quality point of contact and decision maker during New Product Introductions, Technology Transfer and Process Validation activities for Aseptic products Quality review and approval of Process Development and Validation documentation Technical transfer documents Validation Protocols, executed validation documents and reports Provide Quality direction and input at Change Control and Deviation Review Boards and assume QA oversight of change control and Deviation/CAPA records ABOUT YOU - ARE YOUR SKILLS A MATCH? Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G visa or a Stamp 4 visa. Please note that we are unable to provide visa sponsorship. Thank you for your understanding. Apply via this advert or contact Siobhan Cummins on if you have any more questions about this opportunity!

LSC have a great contract opportunity for Quality Assurance CQV to join a leading Biopharmaceutical Facility in Louth. If you have 5 years of experience and are ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Ensure the quality oversight of the qualification/validation activities of all facilities, utilities, equipment, computerized systems, cleaning processes, manufacturing processes, storage areas, controlled temperature units (CTUs) and shipping processes. Ensure that all validation documentation and associated data, including but not limited to; plans, URSs, quality risk assessments, protocols, and reports, are reviewed and approved by QA for conformance to SOPs, specifications and other applicable acceptance criteria. Ensure that all events/deviations, investigations, and change evaluations that occur during qualification/validation activities have appropriate QA oversight, QA review and approval and adhere to SOPs and cGMP requirements. Review SOPs relating to qualification/validation activities. Provision of support in Regulatory inspections and Client audits. Provision of QA Validations expertise to maintain validation status of the facility. ABOUT YOU - ARE YOUR SKILLS A MATCH? B.Sc or B.Eng in a Scientific or Engineering related discipline (e.g. biochemistry, chemistry, engineering). Experience in a Quality Engineering/Quality Assurance/Quality Validations role for Biologics or related pharmaceutical/ medical device manufacturing in a FDA/ EU regulated environment. For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. We apologize for any inconvenience, as visa sponsorship is not available currently. Apply via this advert or contact Cian Marnane on if you have any more questions about this opportunity! Skills: Quality Assurance Commissioning Qualification

Job Description Your New Job Our client, a leading global pharmaceutical company, is currently seeking a Quality Assurance (QA) Specialist to join their team on a contract basis at their state-of-the-art manufacturing site in Carlow. This is an excellent opportunity to work in a high-performing, fast-paced sterile manufacturing environment supporting production teams across a 4-shift cycle. As QA Specialist, you will be responsible for providing quality oversight and ensuring compliance with GMP standards. The role will involve review of batch documentation, supporting investigations, and working cross-functionally with manufacturing and quality systems teams. This role is ideal for someone who has strong attention to detail, a passion for quality, and is looking to grow their experience within a dynamic pharmaceutical setting. Key Duties & Responsibilities Provide day-to-day quality support to production teams, ensuring compliance with GMP standards and site procedures. Perform timely review and approval of batch documentation (EBRs), including line clearance verification. Assist in investigations of deviations, customer complaints, and unplanned events, using systems such as TrackWise. Conduct and report on routine audit readiness and quality metrics to drive continuous improvement and maintain compliance. Participate in spot-checks and walkthroughs on the production floor to monitor adherence to quality standards. Ensure compliance with current GMP, FDA, EMA, and internal quality standards and regulations. Liaise with cross-functional teams (Manufacturing, Engineering, QC) to identify and implement quality improvements. Utilize computerized systems (SAP, MES) for recording, tracking, and reporting quality-related activities. Maintain awareness of industry trends and regulatory updates relevant to sterile manufacturing. What Are We Looking For? Bachelors degree (or higher) in a Science or related discipline. 12 years experience in a QA role within a pharmaceutical manufacturing environment, ideally with aseptic/sterile processing exposure. Strong working knowledge of cGMP and GDP. Experience using quality systems such as SAP, MES, and TrackWise is desirable. Ability to prioritise and manage multiple tasks in a fast-paced setting. Strong interpersonal and communication skills. A proactive mindset with a focus on audit readiness and continuous improvement. Why This Job? Join a world-renowned pharmaceutical leader with a strong reputation for innovation and quality. Gain valuable experience in a sterile manufacturing environment working on a 4-cycle shift pattern. Be part of a collaborative team environment with opportunities to develop professionally. Competitive hourly rate and contract benefits available. Apply for this job now by emailing your WORD formatted CV or contact Jonathan via mobile on By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are kept confidential and will not be submitted to any clients without your knowledge and permission. Please note that due to the expected high volume of applications we can only reply to applicants suitable for the position. We Value Your Trust. Skills: Trackwise cGMP GMP QMS

C&D Foods is one of Europe's leading own label pet food manufacturers producing a range of wet and dry pet foods. C&D Foods has grown to become one of the industry's leading pet food producers. C&D Foods has 9 production facilities across 7 Countries (Ireland, the UK, France, Denmark, Austria, Spain, and The Netherlands) and 2 sales offices located in Manchester and Italy. We currently have an opportunity for a Quality Assurance Technician within our Quality Team in Edgeworthstown, The Role will involve working on 12 hour Shifts 6am to 6pm on the following work pattern Week 1 Monday, Tuesday, Wed, Saturday and Sunday Week 2 Thursday & Friday Week 3 Monday, Tuesday, Wednesday, Sat and Sunday Key Responsibilities Verify Thermal Processes to ensure compliance with food safety standards Conduct Daily Product Evaluations and Quality Testing Perform Good Manufacturing Practice (GMP) Audits across production areas Review and maintain accurate Quality Documentation and Records Collect and manage Product Samples for analysis and traceability Execute Production Line Quality Checks to ensure consistent standards Carry out Glass and Hard Plastic Control Audits to mitigate contamination risks Monitor Pest Control Measures, including bait station inspections Verify Cleaning Procedures to ensure hygiene standards are upheld Perform Metal Detector and Check Weigher Validations Communicate qualityrelated findings and concerns to relevant Department Managers Support and participate in Internal and External Site Audits Any other requirements which may arise to support the quality department including (Cleaning, Pest Control). Skills and Experience A highly motivated and dependable individual with the ability to manage multiple tasks effectively 1-2 years' experience in a similar quality or food manufacturing role Proficient in Microsoft Office applications, including Outlook, Word, and Excel A collaborative team player with a positive and approachable attitude Exceptional attention to detail and a strong commitment to accuracy Excellent verbal and written communication skills Ability to work under pressure, meet deadlines, and adapt to a fastpaced environment 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.