Computer System Validation
590 open positions
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Senior Validation Specialist MsdIRL - Carlow - Carlow, IE 6d Lead, execute, and oversee filter qualification and validation programs for sterile manufacturing processes and equipment to ensure regulatory compliance and operational excellence.
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Lead Engineer, IT Compliance, Data Integrity BristolmyerssquibbBothell - WA - US $118k–$143k6d Lead IT compliance and data integrity programs for GxP computerized systems in Cell Therapy manufacturing, quality, and lab operations.
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QA Specialist ( Equipment Introduction)↗ Berkley GroupCarlow, County Carlow, Ireland 6d Provide quality oversight for the introduction of new equipment, from commissioning and qualification through to validation.
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Quality Engineer II - Validation BaxterRound Lake, Illinois, US $88k–$121k6d Independent quality partner providing oversight and guidance across validation, qualification, and data integrity activities to ensure regulatory compliance for equipment, facilities, utilities, manufacturing processes, and computerized systems.
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Ingénieur Validation Procédés – Production Pharma (H/F) EurofinsVal-de-Reuil, Normandy, fr 7d Validate pharmaceutical manufacturing, cleaning, and packaging processes while coordinating industrial trials and optimizing production workflows.
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Ingeniero de Manufactura I↗ MedtronicCiudad Juárez, CHH, MX 7d Provide engineering support for calibration, equipment qualification, validation, and manufacturing activities in a regulated medical device production environment.
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Quality Engineer II↗ Weil Group, IncPonce, PR, US 7d Execute validation, qualification, and process improvement activities for equipment, processes, and manufacturing systems in a regulated environment.
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Validation Engineer↗ Syner-G Biopharma GroupRemote 7d Develop, execute, and maintain validation lifecycle documentation (CQV, CSV) for equipment, utilities, facilities, and computerized systems to ensure GMP compliance and operational readiness.
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Quality Engineer II↗ Echo Consulting GroupPR, US 7d Execute validation, qualification, and process improvement activities in a regulated manufacturing environment to ensure compliance with quality and regulatory requirements.
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?Validation Engineer↗ Ponce, PR, US 7d Develop, execute, and review validation protocols and documentation for utility systems (Compressors, Chillers, AHUs, Generators) in the Pharmaceutical, Medical Device, and Manufacturing industries.
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?Quality Engineer↗ Ponce, PR, US 7d Execute validation protocols and statistical analysis to ensure compliance with quality and regulatory requirements in manufacturing and engineering.
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Senior Manufacturing Validation Engineer↗ Terumo AorticRenfrew, Scotland, UK 7d Ensuring manufacturing equipment and processes are validated to regulated standards to support customer and business needs.
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Konsult inom Life Science↗ Knightec GroupSödertälje, Stockholm County, Sweden 7d Consultant supporting customers in the Life Science industry to improve production, quality, and project operations through expertise in validation, project management, and process development.
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CSV Engineer (m/f/d)↗ OriseDublin, County Dublin, Ireland 7d Manage GxP Computerised Systems CSV activities, define CSV strategy, and oversee validation documentation for Life Sciences projects.
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Analista Sênior de Qualificação de Equipamentos | Projeto Temporário↗ Jma Plân Engenharia & ConsultoriaItapevi, São Paulo, Brazil 7d Senior Equipment Qualification Analyst responsible for planning, executing, and reviewing equipment and system qualification activities (QI, QO, QD) and CSV/VSC validation in a regulated pharmaceutical environment.
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Ingeniero de Calidad & Validaciones↗ Bepc Inc. - Business Excellence Professional ConsultingApodaca, Nuevo León, Mexico 7d Develop and execute validation protocols (IQ, OQ, PQ) for medical device manufacturing equipment and processes to ensure compliance with GMP/GDP.
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Process Validation Co-Op↗ VantiveCastlebar, County Mayo, Ireland 7d Support process validation, quality systems, and manufacturing operations in a regulated pharmaceutical environment.
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CSV Engineer↗ No deviationSingapore, Singapore 7d Validate Emerson DeltaV automation systems for pharmaceutical and biopharmaceutical manufacturing environments by developing test scripts, executing protocols, and ensuring compliance with GMP and GAMP 5.
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Validation Engineer↗ RemedicaLimassol, Limassol, Cyprus 7d Ensure systems, equipment, utilities, facilities, and instruments are commissioned, qualified, and maintained in compliance with cGMP and regulatory standards throughout their lifecycle.
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Computer System Validation (CSV) Engineer / Specialist↗ Fidelis Talent SolutionsCarolina, PR, US 7d Ensure computerized systems comply with regulatory requirements, data integrity, and quality standards throughout their lifecycle in a regulated GxP environment.
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Técnico/a de Garantía de Calidad en Validaciones y Cualificaciones (CSV/CQV)↗ ChemoAzuqueca de Henares, Castile-La Mancha, Spain 7d Ensuring the qualification status of equipment, facilities, and services, as well as the validation status of processes associated with the manufacturing of injectable products, including aseptic processes, cleaning, and conditioning.
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CSV Engineer↗ SimotechCork, County Cork, Ireland 7d Ensuring validation and compliance of GMP-computerised systems and equipment for a biopharma client through lifecycle validation and data integrity management.
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Senior MES Quality Validation Specialist↗ Amaris Consulting | Part of MantuToronto, Ontario, Canada CA$70k–CA$110k7d Senior Quality approver for Manufacturing Execution System (MES) changes, ensuring GxP compliance and inspection readiness for digital projects in pharmaceutical manufacturing.
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Qualifizierungsingenieur SAT (m/w/d) (Qualification Engineer SAT), BWT Parma Bietigheim BWT Pharma & Biotech GmbHBietigheim-Bissingen, BADEN_WUERTTEMBERG 7d Creating, coordinating, and managing technical project documentation and qualification records (FAT/SAT protocols, risk analyses, URS) for water treatment systems in the Pharma & Biotech industry.
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CQV Engineer – SPOC Utilities & HVAC 80-100% (m/f/d) LonzaCH - Visp 7d Subject matter expert and primary point of contact for the qualification and validation of Utilities and HVAC systems throughout their lifecycle to ensure compliant, reliable, and efficient operation.
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Sr Associate Technical Engineer PfizerUnited States - New York - Pearl River $83k–$138k7d Sr Associate Technical Engineer responsible for implementing and sustaining Continuous Improvement projects and Validation Master Plan elements for clean utilities and equipment cleaning at a pharmaceutical manufacturing site.
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Responsable de Validación de Sistemas Informatizados (CSV)↗ Ambit IberiaBarcelona, Catalonia, Spain 8d Design and implement risk-based strategies for computerized system validation (CSV) in pharmaceutical and life sciences environments, ensuring compliance with GxP regulations.
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Computer Systems Engineer↗ Coalesce Management ConsultingSingapore, Singapore 8d Lifecycle management, commissioning, qualification, and validation of automated equipment and computerised systems in a GMP-regulated pharmaceutical manufacturing environment.
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Validation Engineer FreseniusglobalGrand Island, NY, US $63k–$85k8d Validates and revalidates new or modified products, equipment, and systems in a pharmaceutical manufacturing environment.
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CSV Engineer↗ No Deviation Pte. Ltd.Singapore, S00, SG 8d Validate Emerson DeltaV automation systems in pharmaceutical/biopharmaceutical manufacturing environments by developing test scripts, executing protocols, and ensuring compliance with GMP/GAMP 5.
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Engineering CQV SME - Sterilisation / Autoclaves↗ Bristol Myers Squibb UK & IrelandCounty Dublin, Ireland 8d Senior Engineering CQV Subject Matter Expert specializing in autoclave qualification and equipment temperature mapping for biologics and sterile drug products.
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QA Associate - Validation↗ Alliance HealthcareSouth Normanton, England, UK 8d Support business compliance to GDP and GMP regulations ensuring work is completed safely, efficiently, and to agreed quality standards.
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C&Q (Process Development) Engineer↗ Tech Skills Resources (part of the Cpl Group)Monaghan, County Monaghan, Ireland 9d C&Q (Process Development) Engineer supporting pharmaceutical and biopharmaceutical projects across Ireland, the UK, and Europe by optimizing and qualifying critical process systems including sterilization and washing equipment.
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Group Senior Expert - QA IT↗ Randstad SwedenStockholm, Stockholm County, Sweden 10d Senior QA expert ensuring quality and compliance for computerized systems in the manufacturing of biological medicines, serving patient safety and product quality.
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Senior Ecompliance Manager↗ CdmsXico, Veracruz, Mexico 10d Lead eCompliance strategy for GxP-regulated computerized systems and emerging technologies, ensuring data integrity and regulatory compliance across the system lifecycle.
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TÉCNICO DE PRODUCCIÓN (Cualificaciones de sistemas HVAC, calibraciones y cualificaciones térmicas y/o de aire)↗ QualipharmaAlcobendas, Community of Madrid, Spain 10d Calibration and qualification technician for HVAC, thermal, and air equipment in the pharmaceutical industry.
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