Quality Assurance Systems and Validation Specialist

Position OverviewThe Quality Assurance Systems and Validation Specialist plays a critical role in ensuring that all Good Manufacturing Practice (GMP) related changes, systems, and validation processes meet regulatory standards and internal quality benchmarks. This position serves as a subject matter expert in change control, validation, and quality systems, …

Cytokinetics is a late-stage biopharmaceutical company based in Dublin, Ireland, focused on cardiovascular treatments. The team specializes in discovering, developing, and commercializing muscle activators and inhibitors that address diseases affecting cardiac muscle performance. With a strong foundation in muscle biology and mechanics, Cytokinetics develops small molecule drug candidates to improve myocardial muscle function and contractility. Role Overview The Director of Quality Assurance, Alliance Management will play a central role in supporting Cytokinetics’ global partnerships. This leader ensures that quality and compliance standards are established and maintained across all in-licensing alliances with regional partners. Key Responsibilities Lead and coordinate Quality Assurance activities across partner relationships. Ensure all partnerships comply with global regulatory requirements and Cytokinetics’ internal quality standards. Act as the primary liaison between Cytokinetics and its strategic partners for quality-related matters. Support the onboarding of new alliances and manage ongoing quality aspects of established collaborations. Collaboration This position reports to the Head of Quality Assurance Operations. Regular collaboration occurs with Alliance Management, Technical Operations, Regulatory CMC, and other cross-functional teams.

Are you an experienced Software Engineer in Test, Test Engineer, or Test Analyst with a passion for both manual and automated testing? Join our dynamic agile team at Version 1, where you'll play a pivotal role in helping our clients achieve their business transformation goals through comprehensive testing strategies.Your responsibilities will include collaborating with cross-functional teams to uphold quality standards, validating and analyzing large data sets using SQL, and developing insightful reports and dashboards with tools like SSRS and Power BI. Additionally, you will support our test management processes using QMetry and contribute to our automation testing initiatives, particularly focusing on API testing with Karate.Be part of a culture of knowledge-sharing and collaboration across diverse regions and functions.

As Europe's premier dedicated data center delivery partner, Winthrop Technologies provides comprehensive turnkey solutions, from initial design to final construction and commissioning. Based in Dublin, we manage projects across the continent, establishing ourselves as the most reliable name in the industry.We are excited to announce an opening for a QA/QC Engineer on a significant data center project in Dublin 15. This position presents an outstanding opportunity to play a pivotal role in ensuring quality across Civil, Structural, Architectural, Mechanical, and Electrical domains for a complex, high-value initiative.Role OverviewIn this role, you will report directly to the Project Quality Manager and collaborate closely with Construction Managers, Project Managers, and discipline engineers. Your primary responsibilities will include implementing and upholding stringent Quality Assurance and Quality Control measures for both CSA and MEP works.Your efforts will guarantee that all construction operations align with project specifications, drawings, relevant standards, legal requirements, and client expectations.Key ResponsibilitiesGeneral QA/QC ResponsibilitiesFormulate, deploy, and sustain project-specific QA/QC procedures across CSA and MEP disciplines.Oversee and assess site activities to verify compliance with drawings, specifications, industry standards, and regulatory mandates.Keep meticulous and current quality records, registers, certifications, and inspection documentation.Foster a robust culture of quality, safety, and compliance throughout the project.CSA ScopeExamine and validate Civil, Structural, and Architectural works, including concrete, steel, finishes, and building envelope components.Review subcontractor method statements, Inspection & Test Plans (ITPs), and material submissions for CSA projects.Generate and manage Non-Conformance Reports (NCRs) and ensure prompt resolution of corrective actions.Ensure that materials and workmanship conform to approved specifications and quality benchmarks.MEP ScopeInspect and confirm Mechanical and Electrical installations, including HVAC systems, electrical distribution, containment, piping, fire protection, and related systems.Review and oversee MEP ITPs, commissioning documentation, and vendor quality submissions.Collaborate with commissioning teams to meet quality requirements before system handover and energization.Witness testing, inspections, and commissioning activities as needed.Coordination & ReportingWork closely with construction teams, design teams, subcontractors, and vendors to address quality-related matters.Provide technical guidance to site teams to ensure the effectiveness of corrective actions.

Version 1 is looking for a Quality Assurance/Test Analyst in Dublin. This position centers on maintaining the quality and dependability of software products. Role overview The analyst will work closely with teams from different disciplines to support software development and delivery. The main focus is on testing and quality checks throughout the project lifecycle. What you will do Design test plans tailored to project requirements Execute test cases to validate software functionality Spot and document areas where improvements are needed Collaborate with cross-functional colleagues to resolve issues Location This role is based in Dublin.

Why Choose PlayStation?At PlayStation, we believe in creating extraordinary gaming experiences, and we value our team as much as we value our players. As a recognized leader in the global entertainment industry, we proudly create innovative products such as PlayStation®5, PlayStation®4, PlayStation®VR, and PlayStation®Plus, along with acclaimed software titles from PlayStation Studios.Our commitment to fostering an inclusive and diverse environment empowers our employees and encourages everyone with a passion for technology and play to explore our opportunities and join our expanding global team.The PlayStation brand is a part of Sony Interactive Entertainment, a subsidiary of Sony Group Corporation.Job Title: Quality Assurance Automation EngineerLocation: Dublin, IrelandThis role focuses on ensuring the quality, performance, and reliability of Adobe Experience Manager (AEM) applications through a blend of manual and automated testing. You will collaborate closely with cross-functional teams in an agile environment to validate new features and support scalable, secure product development. Your contributions will be vital in delivering high-quality releases by identifying defects, enhancing test coverage, and improving continuous integration practices.Key Responsibilities:Develop, execute, and maintain manual and automated test plans and scripts for AEM functionalities and performance.Tackle complex business challenges while ensuring product scalability, security, and performance.Conduct thorough functional, regression, and performance testing on new or enhanced application features.Collaborate in an agile, highly interactive environment with globally distributed engineering teams, including architecture, product management, quality assurance, and operations.

As a Quality Assurance Analyst at airapps in Dublin, the focus is on upholding the quality and reliability of the company’s software products. This position works in close partnership with the development team to create, carry out, and refine test plans. Role overview This role centers on reviewing software solutions to ensure they meet established standards. Day-to-day work includes designing and executing tests, then sharing feedback that supports ongoing product improvement. Collaboration Regular interaction with developers is expected, with the goal of identifying issues early and contributing to the delivery of well-tested, dependable software. Impact By applying quality assurance expertise, this role helps airapps maintain high standards throughout the software development cycle.

Join Olema Oncology, a pioneering company committed to developing innovative treatments for breast cancer and beyond. Our flagship program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently under development for metastatic breast cancer, showcasing tremendous potential as both a monotherapy and in combination therapies for ER+/HER2- metastatic breast cancer. Additionally, our follow-on candidate, OP-3136, is a potent KAT6 inhibitor poised to lead the market.At Olema, we drive scientific breakthroughs through our unwavering support, motivation, and challenge of one another. We believe that by prioritizing our people, we can achieve unparalleled results. If you are ready to be part of an unstoppable force and make a meaningful impact for our patients, your career, and beyond, we invite you to join us.Discover more about us in our latest corporate deck and presentations.About the Role >>> Associate Director, GMP Quality – Qualified PersonAs the Qualified Person (QP), reporting to the Senior Director of Quality Assurance based in San Francisco, California, you will be instrumental in ensuring that our Clinical and Commercial products are manufactured, tested, and released in accordance with the regulatory requirements of the European Union. Moreover, you will facilitate the certification process by QPs in the United Kingdom and Israel, ensuring compliance with U.S. standards.Your responsibilities will include conducting audits of Suppliers and Contract Service Providers across the European Economic Community and other regions, while closely monitoring any changes to European regulatory requirements. You will also host inspections conducted by the Health Product Regulatory Authority (HPRA) and other Competent Authorities within the European Union. As a key contributor to our annual Quality System reviews—including Quality Management Review (QMR) and Annual Product Reviews (APRs)—you will collaborate with our European CDMOs and assist in managing European Product Complaints.This position is based in our Dublin, Ireland office and will require up to 25% travel, which may include some international trips.Your primary responsibilities will encompass:Batch CertificationEnsuring all manufacturing and testing activities adhere to approved procedures, Investigational Medicinal Product Dossiers, and regulatory standards.Overseeing that outsourced manufacturing and testing activities comply with GMP regulations.

Position OverviewWe are in search of a highly skilled Senior CQV / Lab Equipment Validation Engineer with at least 5 years of laboratory experience to contribute to a dynamic equipment installation and qualification project. This hands-on role encompasses the commissioning, qualification, validation, and documentation of laboratory instruments and systems. The ideal candidate should have the capability to work independently, effectively manage timelines, and produce high-quality validation packages that meet GMP, regulatory, and project specifications.Key ResponsibilitiesConduct commissioning, installation verification, IQ, OQ, and documentation for laboratory instruments and equipment.Oversee validation activities to ensure adherence to GMP, GAMP5, Annex 11, 21 CFR Part 11, and internal quality standards.Formulate, evaluate, and implement validation protocols, testing scripts, risk assessments, and summary reports.Collaborate closely with Engineering, Lab IT, Quality Control, Quality Assurance, and external vendors to synchronize installation and qualification efforts.Diagnose equipment issues, escalate technical challenges, and ensure prompt resolutions to maintain project schedules.Guarantee all validation deliverables align with regulatory standards and audit criteria.Keep meticulous records and ensure systems remain validated throughout their lifecycle.Assist in managing change controls, deviations, investigations, and CAPA related to validation processes.Work autonomously to handle workload and deliver assigned equipment qualification packages within strict deadlines.

Join AbbVie, a global biopharmaceutical company, as an Aseptic Product Quality Manager. In this pivotal role, you will ensure the highest standards of product quality in aseptic processes, driving compliance and operational excellence.

Cytokinetics develops therapies for cardiovascular conditions, focusing on muscle activators and inhibitors that target cardiac muscle function. The company’s work centers on small molecule drug candidates to improve heart muscle performance and contractility. Role overview The Senior Quality Associate (Contractor) supports the Quality Department by handling documentation, complaints, reporting, and administrative tasks. This position helps streamline operations and maintain compliance, allowing other QA professionals to focus on oversight and higher-level quality issues. The department operates in a regulated environment with growing needs in documentation, customer assurance, and reporting. There is a particular emphasis on complaints management, CMO scorecard development, and compliance verification as administrative demands increase. What you will do This contractor role is part-time, requiring about 20 hours per week. Main responsibilities include: Document Creation and Execution Support Prepare, format, and maintain QA documentation using Veeva. Coordinate document lifecycle activities, including review and version control. Ensure all documents comply with internal standards. Complaints Management Support Initiate and track customer complaints. Support data entry, documentation, and follow-up for complaints. Maintain audit-ready records of complaint activities. CMO Scorecard Development Assist with gathering and consolidating data for CMO performance metrics. Prepare and format scorecards and reports. Check for consistency and accuracy in reporting. Distribution and Quality Disposition Support Coordinate the distribution of quality-related documentation. Location Dublin, Dublin, Ireland

Senior Validation Engineer________________________________________CAI Overview:Are You Prepared to Make an Impact?Established in 1996, CAI is a leading professional services organization that has expanded year after year, now boasting a global workforce of nearly 700 professionals. We specialize in delivering critical solutions within the Life Sciences and Mission Critical sectors, providing comprehensive services including commissioning, qualification, validation, project management, and consulting to ensure operational readiness in FDA-regulated and other high-stakes environments.Our mission is straightforward yet powerful: we strive to be the trusted partner for our clients, assisting them in crafting a better working world and enhancing the human experience.At CAI, we are dedicated to upholding our Foundational Principles both in our professional and personal lives:• Integrity is our core value• We support one another• We contribute to our community• We invest in our futureWe are relentless in our pursuit of excellence, constantly pushing the envelope and exceeding expectations. From our inception, we've dared to challenge the status quo, not only setting industry standards but redefining them entirely. Our innovative mindset and creative methodologies allow us to thrive at the intersection of wisdom, technology, and humanity. For us, operational readiness is not just an objective; it is a way of life. We believe in proactive engagement, meticulous execution, and a commitment to continuous improvement.________________________________________Job Title: Senior Validation EngineerDepartment: Commissioning, Qualification & ValidationReports To: Senior Validation ManagerJob Type: Full-TimeLocation: Dublin, Ireland________________________________________Job Summary:As a Senior Validation Engineer, you will spearhead commissioning, qualification, and validation initiatives for packaging and combination product assembly lines, ensuring adherence to Good Manufacturing Practices (GMP), data integrity, and regulatory compliance. You will collaborate with project teams to formulate and implement validation protocols, oversee documentation processes, coordinate resources, and ensure timely execution of CQV activities. Your early involvement in projects will provide essential design insights, facilitate vendor coordination, and address potential risks, all while partnering with cross-functional teams to achieve optimal outcomes.________________________________________Key Responsibilities:Lead and manage end-to-end validation processes in a GMP environment.

Company: National Vehicle Distribution (NVD) Location: Baldonnell, Dublin About National Vehicle Distribution National Vehicle Distribution (NVD) is a family-owned business established in 1980. The company specializes in the efficient distribution of vehicles for manufacturers, handling transportation, storage, and vehicle enhancement before delivery. NVD has consistently adopted new technologies in the Finished Vehicle Logistics (FVL) sector, driving efficiency and delivering cost and time savings for clients. The team values continuous improvement and ongoing advancement in all operations. Role Overview: Quality Specialist This position suits an experienced professional from the automotive sector, ideally with a background in Panel Beating or Bodyshop work, who is ready to move away from hands-on technical tasks. The initial focus will be on conducting detailed Quality Control (QC) inspections to support and raise operational standards across the business. As the role develops, responsibilities will broaden to include Quality Assurance (QA) activities. This involves helping to design, implement, and audit the company's Quality Management System (QMS) in line with ISO 9001 requirements. Key Responsibilities Carry out thorough Quality Control inspections on vehicles and processes. Support the improvement of operational standards across logistics and enhancement services. Assist in the development and maintenance of the Quality Management System (QMS). Participate in audits and ensure compliance with ISO 9001 standards. Preferred Background Experience in the automotive industry, especially Panel Beating or Bodyshop operations. Interest in transitioning from hands-on technical work to a quality-focused role.

About MannaAt Manna, we are revolutionizing delivery by taking it to the skies. Our ambitious mission is to provide high-speed suburban delivery that is not only affordable but also environmentally friendly and safe. We engineer our own aviation-grade drones to deliver a variety of products, from food and coffee to groceries, directly from local stores to customers' doors within minutes.Our team is driven by impact, focused on safety, and embraces the idea that the best solutions emerge from authentic collaboration. We thrive in a fast-paced environment, fueled by passion and a commitment to growth, constantly seeking to improve in everything we do.If you aspire to create world-changing technology that makes a real difference (and enjoy some fun along the way), you'll find your home here.Welcome to Manna — where we deliver the future.Role PurposeAs a Quality Engineer at Manna, you will report directly to the Head of Quality and serve as the main quality assurance presence on-site. Your key responsibility will be to oversee the complete quality lifecycle of our drone manufacturing process — from incoming inspections to in-process checks and final product verification. You will manage inspections of components and materials, address nonconformance reports (NCRs), and collaborate with suppliers, manufacturing, and engineering teams to identify and rectify quality issues at their source.This role encompasses both hands-on inspection on the shop floor as well as supplier quality management including corrective actions. You will have a significant role in establishing Manna's quality management infrastructure from the ground up.Key Responsibilities• Conduct incoming inspections of all purchased components and sub-assemblies against established acceptance criteria, overseeing the physical quarantine, labeling, and disposition of materials through the Incoming Quality Control (IQC) process.• Analyze supplier documentation (certificates of conformance, material certifications, dimensional reports) during incoming inspections to pinpoint recurring quality issues.• Perform in-process inspections at designated manufacturing checkpoints, ensuring process adherence, and collaborate with production teams to manage and resolve in-process nonconformances.• Execute final inspections of finished products before shipment, verifying compliance with applicable drawings, specifications, and acceptance test procedures to prevent the release of non-conforming products.• Generate NCRs for all identified nonconformances — incoming, in-process, and outgoing — and oversee the entire NCR lifecycle from issuance through root cause analysis, corrective action, verification, and closure.• Serve as the primary quality liaison for the manufacturing team and component suppliers: communicate rejections with supporting evidence, review supplier root cause analyses and corrective action plans, and ensure timely resolution of issues.

Anduril Industries is a pioneering defense technology firm dedicated to revolutionizing the military capabilities of the U.S. and its allies through cutting-edge technology. By integrating the innovative expertise, technology, and business practices of leading companies into the defense sector, Anduril is reshaping the design, production, and distribution of military systems. Our advanced systems are powered by Lattice OS, a sophisticated AI-driven operating system that transforms an array of data streams into a real-time, three-dimensional command and control center. As global strategic competition intensifies, Anduril remains steadfast in delivering state-of-the-art autonomy, artificial intelligence, computer vision, sensor fusion, and networking technologies to military operations in a matter of months, not years.About The Team:The Voyager team at Anduril Industries is a dynamic engineering and design division with extensive experience in creating innovative computing and communication solutions tailored for the network edge. This specialized team excels in merging enterprise networking capabilities from global IT leaders with bespoke hardware and software platforms that meet the highest environmental standards.We are currently looking for a Manufacturing, Quality & Test Technician to join our Quality & Test team. This position will primarily involve working at our manufacturing facility in Galway with travel to Dublin. You will be tasked with ensuring rigorous testing of our systems to meet stringent quality standards, thereby guaranteeing that we consistently deliver top-notch products to our customers. Additionally, you will play a crucial role in achieving our production throughput requirements. This role demands creative problem-solving abilities to tackle challenging testing issues and drive continuous improvements in our automation processes, user interfaces, and data analysis methodologies.

Join Atlean World, a pioneering HR SaaS consultancy dedicated to fostering multicultural workplaces, as we enhance the recruitment journey for multilingual markets. As a Quality Reviewer, you will play a pivotal role in ensuring the highest quality standards in content moderation.Your Future Awaits, Unbounded! Seize the opportunity to work in vibrant Dublin, Ireland in the role of Quality Reviewer!Why the Quality Reviewer Position is Ideal for Your Growth:Experience the diverse culture of DublinRepresent an esteemed global brandAccelerate your career with fast-track development opportunitiesYour Daily Responsibilities:As a Quality Reviewer, you will:Evaluate content adherence to established policiesIdentify and escalate policy violationsEnsure consistency and quality in every reviewAct as a brand ambassador for a worldwide organizationQualifications:Fluent in Spanish (LATAM) and proficient in EnglishTechnologically inclined with a passion for the latest innovationsCustomer-focused attitude; prior experience is a plus but not essentialExceptional communication skillsHigh level of empathy and understandingBenefits of Joining Us:Vibrant lifestyle in DublinCareer growth with permanent contracts post-trainingAdditional perks including healthcare insurance, pension contributions, bonuses, and more.Make Your Next Career Move Without Limits!

Location: Dublin Contract: Specified Purpose (12 months maternity cover) Reports to: National Training & Quality Manager About the Irish Red Cross Society The Irish Red Cross Society is part of the International Red Cross and Red Crescent Movement, the world's largest independent humanitarian network. Guided by the Fundamental Principles of Humanity, Impartiality, Neutrality, Independence, Voluntary Service, Unity, and Universality, the organization provides impartial support to vulnerable communities in Ireland and internationally. Role Overview The National Training Quality Administrator provides key administrative support to the National Training and Quality teams. This role focuses on maintaining quality processes and ensuring compliance with PHECC Quality Review Framework (QRF) and Governance Validation Framework (GVF) standards. Main Responsibilities Maintain the IRC Quality Management System (QMS) platforms, including MS SharePoint and Moodle, keeping information accurate and current. Oversee the register of policies, procedures, protocols, and guidelines (PPPG), following up on review schedules as needed. Generate reports for privileging, practitioner operational registers (POR), qualifications, and mailing lists. Update training course materials and presentations to reflect Irish Red Cross standards. Update the IRC published training calendar on a regular basis. Create and process MS Forms for events and data collection. Support meetings by taking minutes, tracking action points, and engaging with committees such as the National Training Coordinator (NTCO), Training Working Group (TWG), and Quality Assurance Working Group (QWAG). Prepare annual applications for Controlled Drugs to the Health Products Regulatory Authority (HPRA) for review by the National Training Compliance Officer. Ensure accurate data entry and filing of Patient Care Report (PCR) and Audit Care Report (ACR) forms. Compile and prepare information for internal clinical audits as required. Contribute to achieving the goals of the Irish Red Cross. Participate in training and development activities as needed.

Join our dynamic team at Sonsoft Inc. as a Manhattan WMS & WMOS Specialist. In this role, you will leverage your expertise in warehouse management systems to optimize our clients' operations, ensuring streamlined processes and increased efficiency. You will collaborate with cross-functional teams to implement and support advanced Manhattan solutions that drive business success.

Role overview airapps is looking for a QA Engineer based in Dublin. The main focus of this position is to help maintain and improve the quality and performance of airapps' applications. Collaboration with the development team is central, with involvement in both planning and hands-on testing activities. What you will do Design and execute test plans for both new features and existing functionality Work closely with developers to spot and address issues early in the development cycle Verify that products meet quality standards prior to release

Role Overview AbbVie is hiring a Laboratory Quality Control Supervisor in Dublin. This position leads laboratory operations with a focus on meeting quality standards and regulatory requirements. The supervisor plays a key part in guiding quality initiatives and improving laboratory processes.