Quality Control Technician at Catalyx | Cork

Catalyx is actively searching for a dedicated Validation Engineer to become a key member of our team, working directly at our customer site in Cork.About Us:At Catalyx, we are a pioneering company in machine vision and automation, committed to merging technology and human expertise to elevate global manufacturing and logistics to unprecedented standards of quality and efficiency. With over three decades of experience, our team has been transforming operational processes across highly regulated sectors by innovating new technological applications and providing expert support. Operating from 9 global offices with a team of over 550 professionals, we have successfully executed more than 3,000 projects and continue to tackle unique challenges with a forward-thinking approach. Discover more about us at www.catalyx.ai.Your Role:As a Validation Engineer, you will play a vital role in supporting commissioning, qualification, and validation processes within a GMP-regulated manufacturing setting. Reporting to the CQV Manager, you will collaborate with cross-functional teams to ensure that all systems, utilities, laboratory equipment, and manufacturing processes are compliant and validated throughout their lifecycle.This role requires the maintenance of existing validated systems and active involvement in the implementation of new systems and process enhancements across both manufacturing and laboratory environments.Key Responsibilities:Facilitate validation activities across utilities, equipment, analytical systems, and facilities in a GMP-regulated manufacturing environment.Assist in planning and executing qualification activities, including FUE Qualification, Computerized System Validation (CSV), and validation for New Product Introductions and change initiatives.Contribute to the creation and upkeep of Validation Master Plans, validation protocols, reports, and related documentation.Ensure validation compliance for existing systems and equipment, maintaining alignment with regulatory standards and site procedures.Support the qualification and validation of critical systems, including HVAC, temperature-controlled environments, cleaning and steaming systems, autoclaves, and associated process utilities.Prepare, review, and facilitate the approval of validation documentation, including protocols, reports, change controls, deviations, and CAPAs.Coordinate validation efforts with cross-functional teams including Manufacturing, Process Development, Quality Control, Quality Assurance, and Regulatory Affairs.

Catalyx is seeking an IT Validation Specialist to work on-site at a client location in Cork. This position centers on supporting pharmaceutical operations, with a strong emphasis on ensuring IT systems and software meet regulatory and operational standards. Role overview The IT Validation Specialist will work within a pharmaceutical environment, focusing on computer system validation (CSV) and compliance. The role involves applying industry best practices to ensure IT infrastructure aligns with both regulatory requirements and operational needs. What you will do Validate IT systems and software to confirm compliance with regulatory and operational standards Apply computer system validation (CSV) principles in a regulated setting Support compliance activities for IT infrastructure and related technologies Requirements Experience with IT infrastructure and computer system validation Background in regulatory compliance, preferably in pharmaceuticals or other highly regulated sectors Catalyx specializes in operational process science and supports organizations in R&D, production, packaging, and delivery across North America and Europe. Formed in 2022 from the merger of CXV Global (Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies, Catalyx draws on more than 30 years of experience helping production-focused, highly regulated industries improve efficiency, performance, and safety. Learn more at www.catalyx.ai.

Catalyx is on the lookout for a dedicated Project Engineer to enhance our team on-site in Cork. About Us:Catalyx is a leader in optimizing operational processes, with a strong presence across North America and Europe. Our expertise lies in automating and servicing R&D, production, packaging, and delivery workflows globally. Formed in 2022 through the merger of CXV Global (Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies, we boast over three decades of experience in helping organizations in production-intensive, highly regulated sectors improve their operational efficiency, performance, and safety. Explore our comprehensive suite of solutions at www.catalyx.ai. Your Role:As a key contributor to our commitment to delivering top-tier lifecycle services to regulated and high-risk markets, you will collaborate with life sciences and other highly regulated organizations. Your role will empower them to boost efficiency and pursue success. We are committed to developing our on-site teams to further support our customers' operational advancements. Key Responsibilities:Oversee and ensure the timely and budget-conscious delivery of engineering projects while meeting all safety and quality standards.Define new engineering projects and obtain necessary capital approvals.Lead and engage in commissioning and qualification tasks for current and upcoming projects.Maintain clear communication with management and project stakeholders.Collaborate with specialist trades and departments.Manage project interfaces with other projects and departments effectively.Engage with third parties including suppliers, clients, and service providers.Organize and manage project documentation.Conduct cost estimations including creation, tracking, and auditing against actual costs.Manage project schedules, ensuring alignment with current project states and forecasting.Report on project progress and identify risks.Conduct feasibility studies regarding constructability, maintainability, and operability.Manage project resources efficiently.Assess the current condition of systems including structural, E&I, safety, permitting, and documentation.Organize and lead project meetings.Provide project-related training as necessary.

Catalyx is on the lookout for a skilled Maintenance Planner to enhance our operations at our customer site in Cork.About Us:At Catalyx, we are a pioneering machine vision and automation firm dedicated to merging advanced technology with human expertise, enabling global manufacturers and logistics companies to achieve unprecedented standards of quality and efficiency. With a rich legacy spanning over three decades, our team has consistently pushed the boundaries of operational excellence across tightly regulated sectors by developing innovative technology solutions and providing expert support. With 9 offices worldwide, over 550 dedicated professionals, and a portfolio of over 3,000 projects, we possess the capability and ambition to tackle complex process challenges on a large scale. For further details, please visit www.catalyx.ai.Position Overview:The Maintenance Planner will play a critical role within the Maintenance Operations team, coordinating all planned, preventive, and corrective maintenance activities across the site. The ideal candidate will collaborate effectively with Technicians, Engineers, Vendors, and cross-functional partners to ensure that maintenance tasks are scheduled, adequately resourced, and executed in compliance with Good Manufacturing Practices (GMP).Key Responsibilities:Strategically plan and schedule all maintenance operations, including reactive, preventative, and calibration tasks using the site CMMS.Facilitate daily and weekly planning meetings to prioritize work orders and evaluate maintenance plans for precision and efficacy.Partner with the Maintenance Operations Manager and site departments to prepare jobs for secure and efficient execution.Anticipate maintenance workloads, identify resource requirements, and manage vendor activities for specialized tasks.Oversee and manage the maintenance notification backlog in the CMMS, ensuring data integrity and audit readiness.Assess work requests, define scopes, inspect equipment, and estimate labor, materials, tools, and parts necessary for planned work.Plan and aid in the execution of annual maintenance shutdowns.Assist in investigations of equipment failures and engage in root cause analysis initiatives.Complete deviations, Corrective and Preventive Actions (CAPAs), and change controls as required.Develop and maintain standard job plans, maintenance procedures, and scheduling protocols.Generate and report on maintenance KPIs to support ongoing improvement and reliability efforts.Collaborate with Stores and Purchasing teams to ensure resource availability.

Catalyx specializes in automation and intelligence for GMP manufacturing, with a focus on shaping the future of life sciences and industrial automation. The company’s global marketing team is expanding in Cork and seeks a Junior Marketing Executive to help build the Catalyx brand across multiple channels. Role overview This position supports the marketing team by producing content and coordinating marketing campaigns and events. The Junior Marketing Executive works closely with the Global Head of Marketing, gaining direct exposure to strategy and execution in a technology-driven B2B setting. What you will do Create marketing content for digital and print platforms, such as the company website, LinkedIn, sales materials, email newsletters, blog posts, whitepapers, and case studies. Maintain consistency with Catalyx’s brand guidelines, tone, and messaging across all materials. Collaborate with subject matter experts and the sales team to develop compelling stories about Catalyx products and solutions. Who this role suits This role fits a motivated marketing professional looking to grow skills in a technology-focused B2B environment. Direct reporting to the Global Head of Marketing offers hands-on learning and insight into the sector.

This Computer Systems Validation Engineer (Lab IT Focus) position is based in Cork with Catalyx. The role centers on validating laboratory software, instruments, and IT environments in regulated settings. This work connects IT infrastructure and lab operations, ensuring laboratory applications and systems meet compliance and validation standards. Role overview As a CSV Engineer focused on Lab IT, the position involves close collaboration with IT, QA, Lab Operations, and Automation teams. Responsibilities include implementing, validating, and maintaining lab systems to meet both regulatory and internal requirements. Strong technical knowledge of IT systems and laboratory applications is required to succeed in this role. What you will do Lead and execute Computer Systems Validation activities for lab IT systems, including lab software, instruments, and integrated platforms. Draft, review, and approve validation documents (IQ, OQ, PQ) to ensure alignment with lab systems and IT infrastructure. Validate laboratory systems such as LIMS, CDS, ELN, and other GxP-relevant applications to meet regulatory standards. Support installation, configuration, and qualification of lab environments, including instrument software and connected systems. Perform risk assessments on lab system architecture, data integrity, and system interfaces. Work with IT teams on system builds, upgrades, patching, and deployments that impact lab systems to maintain validation status. Troubleshoot validation and system issues to support uninterrupted lab operations. About Catalyx Catalyx has over thirty years of experience in machine vision and automation, supporting manufacturers and logistics firms worldwide. With more than 550 specialists across nine offices, the team has delivered over 3,000 projects. Catalyx advances technology applications and provides technical support to clients globally. More information is available at www.catalyx.ai.

Catalyx is on the lookout for a skilled Validation Engineer to become a vital part of our team at our customer site in Cork.About Us:Catalyx is a pioneering machine vision and automation company dedicated to merging innovative technology with human expertise to empower global manufacturers and logistics firms to attain cutting-edge standards in quality and efficiency. With over three decades of experience, the creators behind Catalyx have continuously refined operational processes in highly regulated sectors through the invention of new technology applications and the provision of expert technical support. Our global presence spans 9 offices, with a workforce of over 550 professionals and more than 3,000 successful projects completed. We possess the expertise and reach to tackle unique process challenges on a large scale and are committed to pursuing what has never been achieved before. For more details, visit www.catalyx.ai.The Opportunity:As a Validation Engineer, you will play an integral role in supporting commissioning, qualification, and validation activities within a GMP-compliant manufacturing environment. Reporting to the CQV Manager, you will collaborate closely with cross-functional teams to ensure that systems, utilities, laboratory equipment, and manufacturing processes remain compliant and validated throughout their operational lifecycle.Your responsibilities will include maintaining existing validated systems and assisting in the implementation of new systems and process enhancements within both manufacturing and laboratory settings.Your Responsibilities:Assist in validation activities across facilities, utilities, equipment, and analytical systems within a GMP-regulated manufacturing context.Participate in the planning and execution of qualification tasks, including FUE Qualification, Computerized System Validation (CSV), and validation support for New Product Introductions and change initiatives.Contribute to the creation and upkeep of Validation Master Plans, validation protocols, reports, and associated documentation.Ensure compliance of validated systems and equipment, maintaining alignment with regulatory standards and site protocols.Facilitate the qualification and validation of critical systems, including HVAC, temperature-controlled environments, cleaning and steaming systems, autoclaves, and related process utilities.Draft, review, and aid in the approval of validation documents, such as protocols, reports, change controls, deviations, and CAPAs.Collaborate with cross-functional teams, including Manufacturing, Process Development, Quality Control, Quality Assurance, and Regulatory Affairs, to coordinate validation activities.

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 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.

Job Title: Test ArchitectReporting To: Chief Product & Technology OfficerRole OverviewThe Test Architect is responsible for developing and managing the comprehensive testing strategy and architecture for all Catalyx software products and platforms. This role ensures adherence to top-tier quality engineering standards and defines a testing vision that supports the rapid delivery of reliable, secure, and high-performing software. The Test Architect provides essential technical leadership to both local and remote testing teams and collaborates closely with development, product management, and QA teams to integrate quality throughout the software development lifecycle (SDLC).Key Responsibilities:Test Strategy & ArchitectureDefine and continuously enhance the enterprise-wide testing architecture, patterns, and best practices for all Catalyx software products.Develop a comprehensive testing strategy that encompasses 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 triaging tests, defining test levels, managing test data, environments, and automation protocols.Shape a long-term automation strategy, including CI/CD integration and the selection of appropriate tools.Eliminate inconsistent testing practices, fragmented approaches, and duplicated efforts across teams.Define what constitutes “meaningful coverage”, establishing quality benchmarks that prioritize reliability, business value, and risk-based testing.Lead initiatives to identify and reduce test redundancy, consolidating low-value tests while safeguarding critical coverage.Promote a shift-left approach, ensuring testability considerations are integrated early in the design and development phases.Test Framework & Tooling OwnershipSelect and standardize testing tools and ensure 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 (e.g., Playwright, Cypress, Selenium, K6, JMeter, Postman).Integrate automation into DevOps pipelines to support continuous testing practices.Mentor and guide test engineers, developers in test, and automation specialists.Oversee the daily operations of local and remote test teams, ensuring clear task ownership, equitable workload distribution, and alignment with sprint, release, and milestone targets.

Location: Cork, Ireland (customer site) Role overview The IT Validation Specialist position at Catalyx focuses on ensuring that IT systems and software comply with regulatory requirements and operational standards. The role sits within the pharmaceutical sector, where adherence to industry regulations and best practices is essential. Main responsibilities Support validation activities for IT infrastructure and software systems. Help maintain compliance with relevant regulations and standards in a pharmaceutical environment. Contribute to computer system validation (CSV) processes and documentation. Requirements Strong background in IT infrastructure and computer system validation. Experience with regulatory compliance, ideally in the pharmaceutical or a similarly regulated industry. Catalyx specializes in optimizing operational processes for the life sciences sector across North America and Europe. The company brings together over thirty years of experience through the merger of CXV Global and Panacea Technologies, focusing on partnership, efficiency, performance, and safety in regulated, production-driven environments. Learn more at www.catalyx.ai.

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.

Catalyx is looking for a Junior Marketing Executive to join the team in Cork. This position supports the global marketing group and focuses on building the Catalyx brand in B2B sectors, especially life sciences and industrial automation. Role overview The Junior Marketing Executive will help create content, coordinate events, and support marketing campaigns across multiple channels and markets. The work involves close collaboration with the Global Head of Marketing and offers exposure to a technology-driven environment. What you will do Develop and refine marketing content for various platforms Assist in planning and delivering events that engage target audiences Support the execution of marketing campaigns to strengthen the Catalyx brand Who this role suits This position suits someone motivated and eager to grow their marketing skills. An interest in B2B marketing, life sciences, or industrial automation will be helpful. The role offers the chance to contribute to meaningful projects and learn from experienced team members.

Location: CorkCompany: Catalyx Catalyx specializes in machine vision and automation for manufacturers and logistics firms across the globe. With a 30-year track record, the team works with highly regulated industries, applying technology and expertise to improve operations. Catalyx operates in nine countries, employs over 550 professionals, and has delivered more than 3,000 projects. More details can be found at www.catalyx.ai. Role overview The Computer Systems Validation Engineer - Lab IT Systems plays a key role in validating laboratory software and instrumentation within a regulated environment. The position bridges IT infrastructure and lab operations, ensuring that applications, instruments, and supporting systems comply with validation and regulatory standards. Collaboration with IT, Quality Assurance, Laboratory Operations, and Automation teams is central to this role. Strong technical understanding of both IT systems and laboratory applications is essential. Main responsibilities Lead and execute Computer Systems Validation (CSV) activities for Lab IT Systems, including laboratory software, instruments, and integrated platforms. Prepare, review, and approve validation documentation such as Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), ensuring these align with laboratory systems and IT infrastructure. Validate laboratory systems such as LIMS, CDS, ELN, and other GxP-compliant applications to meet regulatory requirements. Support installation, configuration, and qualification of laboratory environments, covering both instrument software and connected systems. Conduct risk assessments related to lab system architecture, data integrity, and system interfaces. Collaborate with IT teams on system builds, upgrades, patches, and deployments that impact lab systems to maintain validated status. Troubleshoot validation and system issues involving laboratory applications and IT systems.

Catalyx, a dynamic and innovative company, is on the lookout for a skilled Project Engineer to become an integral part of our team at our customer site in Cork. About Us:Catalyx is at the forefront of operational process science, providing cutting-edge automation and service solutions for R&D, production, packaging, and delivery processes across North America and Europe. Formed in 2022 through the collaboration of CXV Global (which includes Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies, we leverage over three decades of experience to optimize operational efficiency, performance, and safety for organizations in production-intensive and highly regulated industries. Explore our extensive capabilities and solutions at www.catalyx.ai. Your Role:As a Project Engineer, you will play a pivotal role in delivering exceptional lifecycle services to our clients in the life sciences and other regulated markets. Your expertise will help us drive efficiency and foster success within customer operations. Key Responsibilities:Oversee the timely and budget-conscious delivery of engineering projects while adhering to safety and quality standards.Define and scope new engineering projects, securing necessary capital approvals.Lead and participate in commissioning and qualification activities for ongoing and upcoming projects.Effectively communicate updates to management and project stakeholders.Facilitate collaboration among specialist trades and departments.Manage project interfaces with other projects and departments to ensure seamless execution.Coordinate with third parties including suppliers and service providers.Organize and maintain project documentation.Conduct cost estimations and manage budgeting processes.Oversee project scheduling and resource management.Report on project progress and identify potential risks.Conduct studies on constructability, maintainability, and operability.Ensure compliance by checking the current condition of systems.Organize and lead project meetings and training sessions as needed.

Catalyx is on the lookout for a dedicated Tableting Inspector to join our team and contribute to our customer site in Cork.About Us:With over three decades of experience, Catalyx is a pioneering machine vision and automation company that harmonizes technology and human expertise to elevate quality and efficiency for global manufacturers and logistics firms. Our innovative solutions have successfully transformed operational processes within highly regulated sectors, supported by our adept team of technical experts. With a presence in 9 countries and a team of over 550 professionals, we have managed over 3,000 projects, consistently pushing the boundaries of what is possible. To learn more about our services, visit www.catalyx.ai.As a trusted partner, Catalyx delivers top-tier lifecycle services to organizations operating in regulated and high-risk markets. Our unwavering dedication to excellence and innovation empowers life sciences and other stringent industry clients to optimize efficiency and achieve success. We are continually enhancing our on-site teams to better support the evolution of our customer operations.Key Responsibilities:Collaborate with fellow Technicians under the direction of a Team Leader and Area Supervisor.Perform Tablet Inspection and manage Tablet/Product material in accordance with GXP, Safety, and Compliance Standards.Oversee packaging and inspection of client products, Clinical Trial Material, and components.Assist in the operation of line equipment, including Manufacturing and Labeling machines, Cartoners, and Printers in the Packaging area.Conduct routine ERP/MES transactions.Execute routine tasks to support area operations and achieve KPIs.Handle materials, feed lines, and perform cleaning tasks.Follow written Standard Operating Procedures (SOPs), Master Batch Records, and current Good Manufacturing Practices (cGMPs).Adhere to all safety protocols and practices, both individually and within the team.Identify and report any deviations from standard practices.Document any variance or deviation from established procedures.Perform additional support duties as needed.Assist in manual operations, including dispensing, inspection, recording, and cleaning within Manufacturing and Warehouse settings.

Catalyx is actively looking for a dedicated Manufacturing Utilities Technician to join our dynamic team at our customer site in Cork.About Us:Catalyx is a pioneering machine vision and automation company that merges technology with human expertise, enabling global manufacturers and logistics firms to achieve unprecedented quality and throughput. For over three decades, our innovative team has been focused on optimizing operational processes across highly regulated industries by developing cutting-edge technology applications and providing expert support. With nine global offices, a workforce of over 550 professionals, and more than 3,000 projects successfully completed, we possess the capability and vision to tackle unique process challenges on a large scale – committed to achieving the extraordinary. To learn more, please visit www.catalyx.ai.As a trusted partner, Catalyx delivers world-class lifecycle services to regulated and high-risk markets. Our unwavering dedication to innovation and excellence empowers life sciences and other highly regulated organizations to enhance their efficiency and achieve success. We are continually advancing our on-site teams to support the enhancement of customer operations.Key Responsibilities:Handle routine assignments while identifying deviations from standard practices.Adhere to established Standard Operating Procedures (SOPs), Master Batch Records, and current Good Manufacturing Practices (cGMPs).Collaborate with Manufacturing Technicians, guided by a Team Lead, to support manufacturing operations.Manage material movements and perform manual cleaning of equipment.Engage in blending, solution preparation, and excipient addition.Monitor manufacturing equipment and processes.Assist in the manufacturing and inspection of customer products, including Clinical Trial Materials and components.Follow all safety protocols and procedures diligently.Comply with detailed instructions for routine tasks and new assignments.Meet agreed KPIs and metrics.Perform additional duties as required.Record information regarding product movement and handling in a computerized inventory system, ensuring accurate records related to distribution activities.Conduct routine transactions linked to distribution processes via internal and external computer systems.Prepare and ship products from the customer’s distribution center.

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.

Join Our Team as a Senior PhysiotherapistWest Cork Children's Disability Network TeamCoAction West Cork Services(Ref D012)Contract: Specific Purpose - 35 hours per weekThis position covers maternity leave.We Welcome Full- and Part-Time ApplicationsApplication Deadline: Tuesday, 10th February 2026For comprehensive details regarding the position and application submission, please visit our website:https://coaction-west-cork.hirehive.com or email hrgen@coaction.iePosition OverviewThe Senior Physiotherapist will be instrumental in delivering a high-quality, patient-centered physiotherapy service to our caseload within the West Cork Children's Disability Network Team (WCCDNT). The role requires effective communication and collaboration within multidisciplinary teams, alongside a commitment to ongoing professional development and a passion for the role.Candidate ProfilePosition Title: Senior PhysiotherapistLocation: West CorkReports To: Children's Disability Network Manager (or approved designate)Essential QualificationsBachelor of Physiotherapy (Hons.) or BSc in Physiotherapy (Hons) or equivalent qualification.Must be a registered member of CORU.Desirable QualificationsTraining in Postural Management.Experience managing a pediatric caseload with intellectual and/or physical disabilities.Essential Skills & AbilitiesStrong clinical knowledge and commitment to evidence-based practice.Excellent interpersonal and communication skills, with the ability to collaborate effectively.Proven ability to work within a multidisciplinary team environment.Innovative approach to service provision, including effective management of pediatric caseloads.Awareness of personal limitations and readiness to seek assistance when necessary.Commitment to integrating evidence into practice.Demonstrated quality focus and commitment to professional growth.