Lead Test Architect at Catalyx | Cork

Catalyx is on the lookout for a skilled Quality Control Analyst to enhance our team at our customer site in Cork. This role is pivotal in ensuring that our products meet the highest standards of quality and compliance.Key Responsibilities:Conduct thorough reviews and release assessments of primary and secondary packaging components.Complete auxiliary tasks related to quality analysis, including data review, archiving, and collaboration with Materials Management.Lead quality investigations and perform root cause analyses as necessary.Deliver services in a LEAN and 7S environment while adhering to good laboratory practices.Comply with safety and quality protocols and actively participate in internal and external audits.Maintain high standards of laboratory housekeeping.Exhibit strong scientific and GMP documentation skills.Perform additional duties as assigned to support team objectives.Qualifications:A degree in a relevant field coupled with experience in the pharmaceutical industry.Post-graduate qualifications that complement the primary degree are advantageous.Hands-on operational experience in quality laboratories within a dynamic manufacturing setting.Comprehensive understanding of quality management systems, pharmaceutical manufacturing operations, cGLP requirements, and pharmacopeial methods.A solid grasp of applicable quality and compliance regulations.Ability to adapt and remain flexible in a fast-paced environment.Exceptional attention to detail is essential.Application Deadline: Wednesday, April 1st

Catalyx is on the lookout for a skilled Quality Control Analyst to join our dynamic team at our customer's site in Cork. This role is essential in ensuring the highest quality standards are met in our pharmaceutical packaging processes.Key Responsibilities:Conduct thorough reviews and release evaluations of primary and secondary packaging components.Complete auxiliary tasks associated with this analysis, including data review, archiving, and collaboration with materials management.Engage in quality investigations and root cause analyses to drive continuous improvement.Deliver services within a LEAN and 7S framework, while strictly adhering to good laboratory practices.Ensure compliance with safety and quality procedures, and actively participate in internal and external audits as required.Maintain exemplary laboratory housekeeping standards.Exhibit strong scientific and Good Manufacturing Practice (GMP) documentation skills.Perform any additional duties as assigned by the management.

Join our dynamic team at SGS as a Quality Control Analyst, where you will play a critical role in ensuring the quality and compliance of our laboratory testing processes. In this full-time position based in Cork, you will be responsible for conducting thorough inspections and analyses, maintaining quality standards, and collaborating with a team of experts to drive continuous improvement.

Join SGS as a Quality Control Analyst specializing in Chemistry. In this role, you will be responsible for performing quality control tests and analyses in a laboratory setting, ensuring that all products meet the required specifications and standards. You will work closely with the laboratory team to maintain high-quality processes and contribute to our commitment to excellence.

Catalyx is seeking a Quality Control Technician to join the team at a client site in Cork. This position plays a key role in supporting laboratory operations within regulated industries, focusing on quality, safety, and effective collaboration. What you will do Coordinate with team members and other departments to ensure smooth laboratory operations. Complete all required training as outlined in standard operating procedures (SOPs) and safety risk assessments. Carry out preventative maintenance and calibration for laboratory instruments. Keep laboratory equipment clean and in working order. Prepare solutions for quality control testing. Track and procure laboratory consumables as needed. Draft SOPs and safety risk assessments when necessary. Maintain the laboratory in a state of readiness for inspections. Requirements Diploma in a scientific discipline. Strong written and verbal communication skills. Customer-focused approach with accountability for speed, quality, and precision. Self-motivated and able to perform well under pressure. Flexible and adaptable to support a growing organization. Why Catalyx? Catalyx values its people and places emphasis on well-being and professional growth. The company offers a range of benefits and support for employees. Learn more about Catalyx at www.catalyx.ai.

AbbVie is seeking a highly skilled and dedicated Senior Manager of Quality Control Laboratory to join our dynamic team in Cork. In this pivotal role, you will oversee the quality control operations within our laboratory, ensuring that all products meet the highest standards of quality and compliance.Your expertise will drive the implementation of robust quality control processes, the development of team members, and the maintenance of operational excellence. You will collaborate closely with various departments to uphold our commitment to quality and safety in all our products.

Catalyx is seeking a Quality Control Technician to join our team at a client site in Cork. This position plays a central role in supporting quality and throughput for manufacturing and logistics, especially within highly regulated sectors like life sciences. What you will do Work closely with laboratory staff and other departments to coordinate daily lab activities. Complete required training on Standard Operating Procedures (SOPs) and Safety Risk Assessments. Carry out preventative maintenance and calibration of laboratory equipment. Keep laboratory equipment clean and organized. Prepare solutions for quality control testing. Track and order laboratory consumables as needed. Draft and update SOPs and safety risk assessments. Maintain the lab in a constant state of inspection readiness. Requirements Diploma in a scientific discipline. Strong written and verbal communication skills. Customer focus with attention to quality, accuracy, and timely delivery. Self-motivated and able to perform under pressure. Adaptable and flexible to support a growing organization. Working at Catalyx Catalyx values team members and supports both well-being and professional growth. Our company specializes in machine vision and automation, serving regulated industries worldwide. With over 550 professionals and 3,000+ completed projects, we continue to drive innovation in operational processes. Learn more at www.catalyx.ai.

Catalyx is actively seeking a dedicated Quality Assurance Specialist to enhance our team and contribute at our customer site in Cork.This role will follow a rotating weekly shift pattern, ensuring flexibility and adaptability in a dynamic working environment.About Us:Catalyx is an innovative leader in operational process management, specializing in automating and servicing R&D, production, packaging, and delivery processes across North America and Europe. Formed in 2022 through the merger of CXV Global (including Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies, we leverage over three decades of experience to help organizations in highly regulated industries optimize their operational efficiency while ensuring safety and performance. Discover more about our extensive capabilities and solutions at www.catalyx.ai.Your Role:As a Quality Assurance Specialist, you will play a crucial role in delivering world-class lifecycle services to regulated and high-stakes markets. Our commitment to innovation and excellence drives us to empower life science organizations and others in regulated sectors to boost efficiency and achieve success. We are focused on continuously developing our on-site teams to support the advancement of customer operations.Key Responsibilities:Oversee quality assurance at various production stages, including material inspections, in-process controls, and product readiness evaluations.Compile and assess documentation to support product disposition, collaborating closely with operational and quality teams to meet release timelines.Assist in packaging operations through visual inspections and by ensuring adherence to established processes during routine activities.Work alongside cross-functional teams (Manufacturing, Quality Control, Supply Chain, Engineering) to address daily queries and challenges effectively.Contribute to the enhancement of quality systems through change control, deviation management, and CAPA oversight.Review documentation such as batch records, SOPs, and work instructions, ensuring compliance with regulatory and internal standards.Engage in the creation of periodic quality reports and metrics to support trend analysis and ongoing improvement initiatives.Participate in internal audits and readiness assessments to guarantee compliance with site and process requirements.Provide informal coaching and knowledge-sharing on quality processes to empower operational teams to work efficiently within GMP frameworks.Support additional quality-related projects as required.

Are you driven by a passion for delivering exceptional service and showcasing technical expertise? Do you aspire to play a vital role in guaranteeing that consumers enjoy a consistently high-quality product experience? If your answer is yes, this opportunity is tailored for you.The primary responsibility of this position is to maintain and service dispense equipment for our esteemed beverage clients.At CPM, every member of our team plays a crucial role in the overall success of our organization. Our people are the cornerstone of CPM’s value proposition, and as a vital member of our team, you will be expected to contribute significantly to our client delivery. This role demands initiative, a strong customer-focused mindset, and an unwavering commitment to best practices and continuous improvement. A proactive, “can-do” attitude is essential.

Catalyx is actively looking for a dedicated Quality Assurance Specialist to enhance our on-site team at our customer facility located in Cork.This position involves a rotating weekly shift schedule.About Us:Catalyx is at the forefront of operational processes, specializing in delivering automation and services for R&D, production, packaging, and distribution on a global scale. Established in 2022 through the merger of CXV Global (comprising Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies, we have over 30 years of experience in optimizing operational efficiency, safety, and performance in production-intensive and highly regulated industries. Discover more about our capabilities at www.catalyx.ai.Your Role:As a pivotal member of our team, you will play a crucial role in providing top-tier lifecycle services to clients in regulated and high-risk markets. Our unwavering commitment to innovation and excellence empowers life science and other regulated organizations to enhance their operational efficiency and drive success. We are dedicated to developing our on-site teams to support our clients' operational advancement.Key Responsibilities:Oversee quality control throughout various production stages, including material inspection, in-process control, and readiness assessment.Compile and review documentation supporting product disposition, collaborating with operational and quality teams to meet release deadlines.Assist in packaging operations through visual inspections and ensuring adherence to processes during routine activities.Work with cross-functional teams (Manufacturing, Quality Control, Supply Chain, Engineering, etc.) to efficiently resolve daily queries and challenges.Contribute to the enhancement of quality systems via change control, deviation management, and CAPA oversight.Review documentation such as batch records, SOPs, and WI updates, ensuring compliance with regulatory and internal standards.Engage in the preparation of periodic quality reports and metrics to support trend analysis and continuous improvement.Participate in internal audits and readiness assessments to confirm compliance with site and process standards.Share knowledge and provide informal coaching on quality processes to empower operational teams to effectively work within GMP frameworks.

Role OverviewWe are looking for a skilled LabVantage LIMS Consultant to facilitate the implementation and enhancement of LabVantage across our Quality Control laboratories. The ideal candidate will collaborate with international stakeholders, laboratory staff, IT departments, and instrument suppliers to effectively configure, deploy, and optimize LabVantage in compliance with GMP regulations.This position is part of a global initiative to implement LabVantage and may require collaboration across various time zones.Key ResponsibilitiesAssist in the implementation and rollout of LabVantage LIMS across Quality Control laboratory locations.Configure and administer LabVantage modules, including:Sample ManagementStabilityInstrument IntegrationSpecifications & Test MethodsMaster Data SetupPrepare laboratory instruments for integration with LabVantage and facilitate data capture.Collaborate with QC analysts and lab managers to gather and translate business requirements into actionable tasks.Design and implement configurations, workflows, and system improvements.Support Computer System Validation (CSV) activities, including:User Requirements Specification (URS)Functional Requirements Specification (FRS)Installation Qualification/Operational Qualification/Performance Qualification (IQ/OQ/PQ)Traceability matricesEnsure adherence to GxP, ALCOA+, 21 CFR Part 11, and EU Annex 11 compliance standards.Facilitate data migration and harmonization of master data.Troubleshoot system issues and provide Level 2/Level 3 support.Engage with global LabVantage teams and local site stakeholders.Deliver training to users and create Standard Operating Procedures (SOP) documentation.Required QualificationsBachelor’s Degree in Science, Information Technology, Engineering, or a related field.A minimum of 3 years of laboratory experience in a GMP-regulated environment.At least 3 years of hands-on experience with LabVantage LIMS.Strong knowledge of Quality Control lab workflows in pharmaceutical manufacturing.Proficiency in LIMS configuration and instrument interfacing.Familiarity with regulatory requirements (FDA, EMA, MHRA).Experience in working within global, cross-functional teams.Preferred SkillsExperience with global LabVantage implementations.Understanding of SQL and database structures.Experience with middleware or instrument integration tools.Strong documentation skills and effective communication with stakeholders.Capability to work across US/EU time zones as required.

Eurofins Scientific is hiring a Chromatography Analyst in Cork. This role centers on performing chromatography analyses in a modern laboratory setting. It is designed for those starting out in analytical chemistry, including recent graduates and early-career professionals. What you will do Carry out chromatography analyses according to established protocols Operate laboratory equipment and keep precise records Contribute to the delivery of reliable bioanalytical results Who will succeed Candidates with a background in chemistry or a closely related science will fit well in this position. Those at the beginning of their careers or who have recently completed their studies are encouraged to apply.

We are excited to announce an opportunity for a Lab Method System Script Writer and Support Analyst to become part of our Lab IT services at the client site. This role is essential in enhancing laboratory processes through technology.Your initial responsibilities will focus on developing SmartLab scripts for both new and established analytical methods, with comprehensive training provided on SmartLab functionalities. As you grow in this role, you will also tackle Core Application issues, leveraging your technical expertise and problem-solving skills to ensure optimal performance.Key responsibilities include:SmartLab Script Writing- Collaborate with Quality Control Labs (QCL) to create SmartLab scripts that facilitate lab analysts in their testing activities, which include interfacing with instruments, data parsing, and calculations.- Work closely with the QCL E-systems group to conduct thorough testing and verification of scripts prior to implementation.Support Analyst Duties- Provide second-level IT support for critical core applications such as LIMS and Empower.- Analyze, troubleshoot, and document solutions to complex problems.- Liaise with application vendors to coordinate problem resolution and maintain system efficiency.- Monitor laboratory activities to ensure effective use of lab systems while maintaining professional communication in a corporate environment.

Are you an experienced security professional passionate about safeguarding information and managing risks? Join Rubrik as a Senior Security Risk Management Analyst. In this key role, you'll be responsible for identifying, assessing, and mitigating security risks across our organization. You will work closely with various teams to promote security best practices and ensure compliance with our security policies.

Job Title: Test ArchitectReporting To: Chief Product & Technology OfficerRole OverviewAs the Test Architect, you will take charge of the comprehensive testing strategy and architecture, ensuring adherence to top-notch quality engineering standards across all Catalyx software products and platforms. This pivotal role involves defining a visionary testing framework, designing scalable and maintainable test automation frameworks, and empowering teams to deliver reliable, secure, observable, and high-performance software swiftly. You will provide technical leadership and guidance to both local and remote testing teams while collaborating closely with development, product management, and QA teams to integrate quality throughout the Software Development Lifecycle (SDLC) and advocate for the adoption of modern engineering practices.Key Responsibilities:Test Strategy & ArchitectureContinuously define and enhance enterprise-wide testing architecture, patterns, and best practices for all Catalyx software products.Develop a comprehensive testing strategy encompassing functional, non-functional, regression, performance, security, accessibility, and reliability testing.Create and maintain testing blueprints, standards, frameworks, and tools to ensure consistency across teams and alignment with product roadmaps.Establish standards for test triaging, levels, test data management, environments, and automation controls.Shape the long-term automation strategy, including CI/CD integration and tool selection.Eliminate inconsistent testing practices, fragmented approaches, and duplicated efforts across teams.Define “meaningful coverage” and establish quality benchmarks prioritizing reliability, business value, and risk-based testing.Lead initiatives to identify and mitigate test bloat, consolidating redundant or low-value tests while ensuring critical coverage is maintained.Promote a shift-left approach, ensuring testability considerations are integrated early in design and development discussions.Test Framework & Tooling OwnershipStandardize tooling and interoperability across all Catalyx software products and technology stacks.Design scalable automation frameworks for UI, API, and microservices applications.Evaluate and implement new testing technologies and tools such as Playwright, Cypress, Selenium, K6, JMeter, and Postman.Ensure automation is seamlessly integrated into DevOps pipelines to support continuous testing.Mentor and coach test engineers, developers in test, and automation specialists.Oversee daily operations of both local and remote test teams, ensuring clear task ownership, equitable workload distribution, and alignment with sprint, release, and milestone targets.