34 IT Technology jobs in Ireland
Manufacturing Information & Technology Systems Engineer
Posted 12 days ago
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Job Description
Are you looking for a meaningful opportunity to apply the latest emerging technologies to systems that enable the development, design, manufacturing, and distribution of Amgen products? We are seeking a creative, innovative, and strategic technology professional to architect and lead the deployment of Manufacturing Information & Technology Systems, focusing on system integration, automation, data collection, at our Dublin manufacturing facility, in alignment with Industry 4.0 / Smart Manufacturing principles.
**Live - What You Will Do**
As a key member of the Technology and Innovation team, you will drive the development and support of technologies used in our manufacturing operations. This role will collaborate with business owners, vendors, and delivery teams to implement cutting-edge technologies that directly impact how we get products to every patient.
**Responsibilities**
+ Lead the **design and integration** of the Manufacturing Information & Technology ecosystem, ensuring alignment with business goals and IT strategy.
+ Champion **Werum** **PAS|X MES (Level 2 Integration)** with automation systems to enable seamless data flow and real-time operational insight.
+ Configure and maintain **OPC (OLE for Process Control)** connectivity and troubleshoot integration issues between systems.
+ Manage and support **OSI PI Historian** implementation for process data collection, trending, and reporting.
+ **Business partner with Direct Manufacturing, Automation, and Manufacturing Support** teams to identify needs and co-develop digital solutions.
+ Own the **technology roadmap** for manufacturing systems, ensuring long-term scalability, security, and compliance.
+ Collaborate with service owners and platform teams to maintain operational systems and ensure compliance with **cybersecurity controls** .
+ Partner with business units to develop **use cases, user stories, and functional requirements** and design and deliver **Proof-of-Concept** **s** **(POC)**
+ Support **regulatory inspections and internal audits;** ensure audit-readiness through documentation, change management, and validation support.
+ Lead or support **deviation investigations, reactive support, and root cause analysis (RCA)** using structured methodologies.
+ Facilitate **communication and presentations across cross-functional teams** , from technical peers to senior leadership.
+ Stay updated with **industry trends** , fostering knowledge-sharing and external networking to bring innovation into practice.
+ Ensure adherence to **21 CFR Part 11, CSV, SDLC** , and other relevant regulatory and quality frameworks.
**Win - What We Expect of You**
**Basic Qualifications**
+ Master's degree and 4 years of manufacturing or information systems experience, OR
+ Bachelor's degree and 8 years of manufacturing or information systems experience
**Preferred Qualifications**
+ Bachelor's or Master's Degree in Computer Science, Engineering, or Information Systems
+ 8+ years of experience in a manufacturing environment, with 5+ years in pharmaceutical or biotechnology industries
+ Proficiency with Manufacturing Execution Systems (e.g., PAS|X) and data historians (e.g., OSI PI)
+ Experience with OPC setup, SQL, web services, messaging, and data mapping for system integration
+ Familiarity with GxP, change control, validation documentation, and audit processes
+ Strong experience with process automation platforms
+ Excellent communication and presentation skills
+ Strong interpersonal skills with a proven ability to collaborate in team-based, cross-functional environments
+ Ability to lead multiple initiatives and prioritize effectively in fast-paced environments
+ Energetic, self-driven, and passionate about applying technology to improve manufacturing outcomes
**Thrive - What You Can Expect** **From** **Us**
We understand that thriving means different things to different people. At Amgen, we offer:
+ Vast opportunities for learning, development, and internal mobility
+ A comprehensive Total Rewards Plan including healthcare, retirement, and career benefits
+ Flexible work arrangements to support work-life balance
+ A collaborative and inclusive work culture with a powerful mission to serve patients
**About Amgen**
Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.
Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.
Technology Solicitor
Posted today
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Technology Solicitor
Description
We are hiring on behalf of a market-leading law firm for a Senior Associate to join their highly regarded Technology and Innovation group. This is an excellent opportunity to work on cutting-edge technology-related legal matters, advising both domestic and international clients across multiple sectors on a wide range of digital, privacy, cybersecurity, AI, and intellectual property issues.
The team has seen substantial growth and is looking for a talented lawyer to contribute to the continued success of the practice. You'll manage complex and high-value client projects, while also taking a leading role in mentoring and developing junior team members.
Top 3 Things to Know About this Job:
Work on high-profile, innovative technology and digital services legal matters.
Lead a collaborative, multi-disciplinary team on complex projects.
Opportunities for business development, client relationship management, and international secondments.
The Role:
Lead on complex and innovative technology law projects across various sectors.
Manage client advisory matters, including large-scale commercial contract negotiations and drafting.
Advise on key issues including data protection, AI, cybersecurity, digital single market compliance (DMA, DSA), and intellectual property.
Collaborate with internal teams, including the Digital Economy Group, on cross-functional client projects.
Contribute to the development of business opportunities and thought leadership in the technology law space.
Participate in business development opportunities, including international conferences and secondments.
The Person:
Qualified lawyer with 5+ years PQE in technology law or a related field.
Experience in advising on data privacy, cybersecurity, AI, intellectual property, and digital services regulation.
Strong commercial awareness and ability to manage a busy caseload independently.
Proven leadership skills with a commitment to mentoring junior team members.
Enthusiastic about business development and establishing long-term client relationships.
Excellent communication, drafting, and organisational skills.
The Rewards:
Competitive salary and benefits package.
Hybrid working options with a focus on flexibility and work-life balance.
A collaborative, inclusive environment that supports professional growth and development.
Opportunities for career progression and international exposure.
Next Steps:
For more information or to apply for this Senior Associate - Technology role, contact Amy Davis at Hunter Savage for a confidential discussion.
Platform Technology Lead

Posted 1 day ago
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Job Description
The **Platform Technology Lead** will be responsible for establishing and implementing new or revised application systems and programs in coordination with the Technology team. The overall objective of this role is to lead a small team of developer and conduct applications systems analysis and programming activities. They will be responsible for frameworks and platforms and work with development managers and leads in that functional area and ensure common solutions and strategic architecture is consistently implemented across Prime & Clearing & Equities org and broader markets technology. The role requires a comprehensive understanding of multiple areas within a function and how they interact in order to achieve the objectives of the function. Applies in-depth understanding of the business impact of technical contributions. Strong commercial awareness is a necessity. Will be accountable for delivery of a full range of services to one or more businesses/ geographic regions. Excellent communication skills required in order to negotiate internally, often at a senior level.
This is an excellent opportunity for the right candidate to join Citi at an exciting time, make a positive impact and grow your career. Please note this is a hybrid position and you will be required to attend the office 3 days per week.
**What you'll do:**
+ Partner with multiple management teams to ensure appropriate integration of functions to meet goals as well as identify and define necessary system enhancements to deploy new products and process improvements
+ Resolve variety of high impact problems/projects through in-depth evaluation of complex business processes, system processes, and industry standards
+ Provide expertise in area and advanced knowledge of applications programming and ensure application design adheres to the overall architecture blueprint
+ Utilize advanced knowledge of system flow and develop standards for coding, testing, debugging, and implementation
+ Develop comprehensive knowledge of how areas of business, such as architecture and infrastructure, integrate to accomplish business goals
+ Provide in-depth analysis with interpretive thinking to define issues and develop innovative solutions
**What we need from you:**
+ Lead a small team of developers, supervise their tasks and provide technical directions and career coaching
+ Minimum of 8-10 years of hands on development experience
+ At least 5 years of working as a lead developer on JAVA backends
+ Working knowledge of big data platforms and data pipeline development
+ Understanding of design patterns and hand on coding skills .
+ Understanding of latest Java versions along with Executor patterns, Stream API , Lambda etc.
+ Understanding of Linux , Bash and basic scripting along basics like Unix group, Hostgroup.
+ Understanding of RDBMS vs NO SQL vs Columnar Databases. Understanding of the file formats like Parquet , Avro , ORC, Iceberg etc. also required.
+ Experience working on Microservice Architecture , Containerization and Orchestration.
+ Working experience of using telemetry specifically open telemetry , ELK , Grafana , Prometheus etc.
+ Prior work experience working in Capital Markets trade processing is a plus.
+ Ability to adjust priorities quickly as circumstances dictate
+ Demonstrated leadership and project management skills
+ Bachelor's degree/University degree or equivalent experience
+ Master's degree preferred
**What we can offer you:**
By joining Citi Dublin, you will not only be part of a business casual workplace with a hybrid working model (up to 2 days working at home per week), but also receive a competitive base salary (which is annually reviewed) and enjoy a whole host of additional benefits that support you (and your family) to be well, live well and save well. Discover more here. ( these benefits Citi is committed to ensuring our workplace is where everyone feels comfortable coming to work as their whole self every day. We want the best talent around the world to be energised to join us, motivated to stay, and empowered to thrive.
**Sounds like Citi has everything you need? Then apply to discover the true extent of your capabilities.**
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**Job Family Group:**
Technology
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**Job Family:**
Applications Development
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**Time Type:**
Full time
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**Most Relevant Skills**
Please see the requirements listed above.
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**Other Relevant Skills**
For complementary skills, please see above and/or contact the recruiter.
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_Citi is an equal opportunity employer, and qualified candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law._
_If you are a person with a disability and need a reasonable accommodation to use our search tools and/or apply for a career opportunity review_ _Accessibility at Citi ( _._
_View Citi's_ _EEO Policy Statement ( _and the_ _Know Your Rights ( _poster._
Citi is an equal opportunity and affirmative action employer.
Minority/Female/Veteran/Individuals with Disabilities/Sexual Orientation/Gender Identity.
Analytical Technology Specialist

Posted 6 days ago
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Job 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
At our Westport site in Co. Mayo, we are now hiring an Analytical Technology Specialist to join our talented and ambitious team, on a 12 months fixed term contract.
The role centers on conducting Cell-Based Potency Assay (CBPA) testing, ad-hoc investigational & development testing.
With an exciting pipeline of products and a great salary and benefits package, this may be the ideal opportunity to develop your career with an industry leader.
So if you are interested in joining this team, read below to find out more.
In your new role, you will:
+ QC Testing of commercial product via Cell Based Potency Assay and related ELISA methods
+ Routine lab duties including critical reagent qualifications, inventory management and equipment maintenance
+ Interdepartmental co-ordination - support product release, drive completion of defined projects etc.
+ Support and execute Method Transfer and Validation activities associated with key biological drug product projects.
+ Assay performance monitoring and trending
+ Compiling and review of Laboratory documentation (e.g. SOPs, methods, validation documentation etc.).
+ Perform lab duty tasks to maintain a high standard of housekeeping within the laboratory.
+ Support regulatory inspections as required.
+ Supporting Root Cause Analysis Investigations
+ Adhere to and support all EHS procedures and policies.
+ Support and lead Laboratory projects to ensure timelines are met successfully.
Qualifications
To succeed in this role, you will have the following Education and Experience:
+ Bachelors of Science, Master's Degree or Ph.D in a Biological Science
+ Practical experience of mammalian cell culture and basic techniques (Passaging, freeze-down, drug treatments) is an advantage
+ Previous GMP experience is advantageous but not essential
+ Sound scientific/practical understanding of ELISA based methods
+ A clear understanding of working within a regulated environment.
+ Excellent communication and presentations skills, both written and oral.
+ Strong analytical skills with the ability to plan and schedule workloads.
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:
Automation Technology Analyst
Posted 1 day ago
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Technology Delivery Lead
Posted 2 days ago
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Job Description
Staff Additive Technology Engineer

Posted today
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Job Description
Term: 23 months initially
Location: Stryker Anngrove, Cork
Hybrid Working.
**Role Summary:**
This role will collaborate closely with process owners in technology development and key partners on the digital team to define and execute strategies for the seamless integration of new hardware, process improvements, and product workflows into our digital ecosystem.
The successful candidate will support the research, development, testing, and qualification of digital tools in partnership with internal stakeholders and external software developers. They will independently develop solutions to a range of moderately complex technical challenges, applying sound engineering judgment and innovative thinking.
Leveraging the latest engineering techniques, the candidate will contribute to reducing product time to market while ensuring compliance with regulatory requirements, project timelines, and cost targets.
The role also involves building strong working relationships across internal and external teams and may include providing guidance or training to other team members as needed.
**What you will do:**
+ Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.
+ Ensure quality of process and product as defined in the appropriate operation and material specifications.
+ Will select components and equipment based on analysis of specifications, reliability and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols.
+ May lead/support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.
+ Will analyse equipment to establish operating data, conduct experimental test and result analysis. Lead and/or participate in process review meetings.
+ Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches.
+ Provide training for manufacturing team members.
+ Ensure adherence to GMP and safety procedures.
+ Review and approval of validation documentation.
+ All other duties as assigned.
**What you will need:**
+ B.S in Mechanical Engineering or related engineering discipline with 4 or more years' experience or a related Master's degree.
+ Experience translating user needs into process flows and requirements.
+ Ability to develop robust testing plans for new software developments and validations.
+ Strong understanding of additive manufacturing data preparation and build file management.
+ Experience with scripting languages such as python.
+ Experience in automation.
+ Proven track record of working in a team-based environment.
+ Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams. Be open minded with the ability to recognise good ideas.
+ Innovative thinker - should be able to envisage new and better ways of doing things.
+ Good understanding of Design for Manufacturing (DFM), statistical tools, and validation/verification techniques.
+ Excellent analytical skills, ability to plan, organise and implement concurrent tasks.
+ Good knowledge of manufacturing processes, materials, product and process design.
+ Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing.
+ Experience in an FDA regulated or regulated industry beneficial.
+ Excellent attention to detail.
If you are interested in this exciting opportunity please reach out.
#IJ
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
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Sr. Technology Project Engineer

Posted 1 day ago
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Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realise the new science's promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, and other serious illnesses. With a deep and broad pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people's lives.
Amgen Dun Laoghaire (ADL) is a 37,000 square metre aseptic drug product operations facility, specialising in secondary manufacturing activities - Formulation, Vial/Syringe Filling, Lyophilisation and Packaging. The ADL site also includes laboratories and cold chain warehouse capabilities. There is a strong culture of continuous improvement and innovation within ADL to strive for solutions that improve health outcomes and dramatically improve people's lives. Amgen is developing the capability to produce all of its medicines in Dun Laoghaire, helping to ensure continuity of supply of our medicines as we expand internationally.
As a member of the Technology Projects Team, the role will support complex and challenging system Technology initiatives and project delivery.
Key Responsibilities:
- Responsible for supporting all tasks related to the technology system project lifecycle, from solution design to GMP qualification.
- Project management and execution of assigned projects including project prioritisation, resource management, status reporting and external communication.
- Working with various stakeholders to scope projects and ensure requirements are satisfied.
- Critically analysing system design, developing, and recommending continuous improvements in line with the latest technology and regulatory standards.
- Work in a collaborative manner within cross functional teams.
- Lead and support system improvements, development of detailed specification, engineering documents, and standard operating procedures.
- Support new product introductions or new technology introductions by performing engineering assessments, implementing automation system configuration changes and supporting engineering runs.
- Solving complex problems, lifecycle management and operational excellence.
- Develop and manage change control requests per established SOPs and processes.
- Develop detailed specifications, engineering documents, system impact assessments, test protocols and standard operating procedures.
- Perform all tasks with due care and attention ensuring compliance with Good Manufacturing Practices and company requirements, policies and procedures.
- Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations.
- Travel at various times may be required to support execution of projects.
Preferred Qualifications and Experience:
- Bachelor's in electrical engineering or Computer Science, Chemical Engineering, Biotech Engineering or related life science engineering with 5+ years' experience in operations/manufacturing environment.
- Manufacturing automation experience in biopharmaceutical Formulation/Fill/Finish or Active Pharmaceutical Ingredient (API) facilities.
- Excellent control systems automation background focused specifically in design, installation, programming, validation and lifecycle maintenance of automated equipment.
- Experience programming and troubleshooting PLC (e.g. Allen Bradley, Siemens, B&R), SCADA (e.g. IFix, InTouch, Zenon), PCS (e.g. Rockwell Automation Platforms) and Batch Systems (e.g. Factory Talk Batch).
- Industrial Networking experience with ControlNet (CNET), DeviceNet, Profibus etc.
- Experienced in the use of Automation support tool such as RSLinx, RSNetworx, FactoryTalk AssetCentre, ThinManager and OSIsoft PI Data Historian.
- Knowledge of GAMP software development lifecycle, ANSI/ISA-S88 and S95 industry standards, 21 CFR Part 11 and Annex 11.
- Working knowledge of network architecture technologies including TCP/IP, Routing, Switching, Network IDS/IPS, Active Directory, Domain Integration and Firewalls.
- Solid leadership, technical writing, and communication/presentation skills.
- Experience in change control, non-conformance, corrective and preventative actions, and validation practices.
- Experience in developing technology strategies for new product introduction and new technology deployment.
- Ability to translate strategic opportunities and emerging technology solutions into tangible pragmatic executable plans.
- Ability to influence the development of business area strategy and Technology strategy where appropriate.
- Ensure application of corporate blueprint and standards using business drivers to local business needs and project requirements.
- Independent, self-motivated, organised and able to multi-task in project environments.
- Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.
- Proficient in managing relationships with stakeholders, coordinating and collaborating with teams from different departments in order to achieve common goals.
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Senior Specialist HR Technology
Posted 2 days ago
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Tax Technology Consulting Manager
Posted 11 days ago
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