Jobs for csv engineer at Limerick

Overview Role Overview Responsible for Computer System Validation activities within a pharmaceutical manufacturing environment. Responsible for the development and execution of key validation and quality documentation including Qualification Plans, Test Plans, Requirements Traceability Matrices (RTMs), and Validation Summary Reports, ensuring full compliance...

Company Overview: Efor Group is a leader in providing expert engineering solutions to major pharmaceutical and life sciences clients. We are expanding our team as part of an exciting new project in Limerick, and are seeking an experienced CSV Engineer to play a key role in delivering compliant, high-quality systems. Key Responsibilities: Plan, write,...

Job Title: Computer System Validation (CSV) Engineer Location: On-site (Limerick) Role Overview:The CSV Engineer will be responsible for ensuring that all computerised systems within the pharmaceutical environment are validated in compliance with industry regulations and company requirements. This specialist role supports the implementation, qualification,...

Whatis it like to work at SimoTech? With a strong collaborative teamworkculture based on respect, trust, and excellence, we play a criticalpartnering role to our clients’ life-changing supply of products topatients. In return, there is excellent salary, benefits, careerprogression, educational support andmuch more.SimoTech require an DeltaV CSV Engineer to...

Whatis it like to work at SimoTech? With a strong collaborative teamworkculture based on respect, trust, and excellence, we play a criticalpartnering role to our clients’ life-changing supply of products topatients. In return, there is excellent salary, benefits, careerprogression, educational support andmuch more.SimoTech has an excitingopportunity for an...

Why SimoTech What is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust, and excellence, we play a critical partnering role to our clients’ life-changing supply of products to patients.  In return, there is excellent salary, benefits, career progression, educational support and much...

Why SimoTech What is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust, and excellence, we play a critical partnering role to our clients’ life-changing supply of products to patients.  In return, there is excellent salary, benefits, career progression, educational support and much...

We are seeking an experienced MES Engineer to join a growing team supporting the design, implementation, and ongoing enhancement of Manufacturing Execution System (MES) solutions within a regulated manufacturing environment. This role offers the opportunity to work closely with cross-functional teams to digitalize manufacturing processes, improve operational...

Senior Computer System Validation (CSV) EngineerLocation: Limerick, Ireland Job Type: Full-Time Experience: 10+ Years Eligibility: EU Nationals PreferredRole OverviewWe are seeking an experienced Senior CSV Lead to manage validation and compliance activities for GxP-regulated computerized systems within a pharmaceutical manufacturing environment. The role...

Position: Computer System Validation (CSV) Engineer. Location: Munster, Ireland. PACIV, a global leader in industrial automation solutions with offices in Ireland, the United States and Puerto Rico, and serving the Life Science, F&B and Utilities industries, is looking for an experienced CSV Engineer. This is a site-based role. Job Description This role...

Efor Group is seeking an experienced CSV Engineer in Limerick to deliver compliant validation for pharmaceutical projects. You will plan, execute, and oversee IQ/OQ/PQ protocols for GxP systems and lead CSV activities across automation, equipment, and processes.The role requires a strong knowledge of FDA/EMA/ICH guidelines, excellent documentation, and the...

SimoTech in Limerick is seeking a DeltaV CSV Engineer to support a biotech manufacturing facility for a multinational biopharma client. You will validate computerised systems within the process automation framework to ensure compliance with industry standards.The ideal candidate has 5+ years’ CSV experience in pharma, hands-on DeltaV and Siemens PLC...

PACIV in Munster, Ireland, seeks an experienced Computer System Validation (CSV) Engineer for a site-based role in a multinational life sciences environment. You will lead CSV activities for digital manufacturing capital projects, ensuring systems are validated per GAMP5 and regulatory standards. Responsibilities include developing plans, reviewing SDLC...

Project Delivery Partners Pte Ltd in Limerick is seeking a Computer System Validation (CSV) Engineer to ensure computerized systems in pharmaceutical environments are validated and compliant with industry regulations.You will author and execute IQ/OQ/PQ validation protocols, review URS and design documents, manage change control, and support...

SimoTech in Co. Limerick is seeking an experienced MES Validation Engineer to support a digital MES implementation project. You will deliver Digital Batch Records (EBRs/MBRs) on Syncade MES, perform testing, validation, and interface verification with third-party systems in a GMP environment.The role collaborates with MES developers, automation, Quality and...

EFOR is seeking an experienced MES Engineer to join a growing team focused on designing, implementing, and enhancing MES solutions in a regulated manufacturing setting. The role involves working with cross-functional teams to digitalize processes, improve efficiency, and support continuous improvement initiatives.Key responsibilities include transitioning to...

QPTech Ltd. in Limerick is seeking a Senior Analyst – Laboratory IT Systems to support the installation, validation and ongoing maintenance of computerised analytical instrumentation across laboratory and manufacturing environments.The role requires hands-on technical work with Active Directory, CSV, and data integrity controls, collaborating with lab...

SimoTech is seeking a Technical Writer to support a warehouse digitisation initiative for a biopharma client in Co. Cork, Ireland. The role focuses on transitioning from paper to digital systems, creating and updating compliant documentation, and supporting CSV testing activities within a GMP/regulatory framework. You will develop SOPs, work instructions,...

Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support...

Overview PM Group is looking for a Test Automation Engineer to join our team. We are seeking a Test Automation Engineer with proven experience working in a GMP-regulated environment to design, develop, and maintain automated test frameworks for computerized systems supporting GxP operations. The role partners with software engineering, QA, validation, and...