Computer System Validation
590 open positions
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Manager, Validation & Testing↗ Theradex OncologyRemote $130k–$165k4d Leads Computer Systems Validation (CSV), software quality assurance, and testing for GxP and non-GxP systems in oncology clinical trials, focusing on scaling automated testing frameworks.
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IN-Specialist_CSV_ITRA_Advisory_Bangalore PwCBengaluru Millenia, IN 4d Specialist in Computer System Validation (CSV), Software Testing, and IT Compliance supporting audit and assurance services.
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Senior Software V&V Engineer NateraUS $109k–$140k5d Senior V&V Engineer owning verification and validation strategy for bioinformatics pipelines, NGS analysis tools, and lab automation software under IEC 62304 and ISO 13485.
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Validation Engineer JobgetherRemote $110k–$125k5d Lead validation lifecycle activities for equipment, utilities, facilities, and computerized systems in highly regulated pharmaceutical, biotechnology, and medical device environments.
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Tecnico di Convalida – Calibratore Pharma Veolia Environnement SABellaria, Siena, it €25k–€30k5d Execute technical qualification, validation, and calibration of instruments and equipment within pharmaceutical production processes.
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Digital & Data Quality Director - US MsdUSA - Pennsylvania - West Point $173k–$273k5d Lead the Digital and Data Quality organization to ensure compliance and quality of GMP computerized systems, automated manufacturing equipment, and data analysis tools within the pharmaceutical manufacturing division.
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Becario/a en la sección de Quality Validations - Departamento de Calidad↗ RecipharmLeganés, Community of Madrid, Spain 5d Intern role in Quality Validations supporting plant and laboratory qualification oversight within a pharmaceutical manufacturing environment.
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Quality Assurance Manager (m/w/d) Computersystemvalidierung (CSV) Midas Pharma GmbHIngelheim am Rhein, RHEINLAND_PFALZ 5d Planning, coordinating, and implementing validation of computerized systems in compliance with regulations; ensuring legal compliance throughout the validation lifecycle.
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Técnico/a de Cualificación y Validación (CQV) – Industria Farmacéutica (TEMPORAL)↗ BETWEEN GroupBarcelona, Catalonia, Spain 5d Qualification and Validation (CQV) Technician supporting pharmaceutical manufacturing lines and equipment qualification.
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Manager, QA Validation Oversight↗ RegeneronNew York, NY, US $110k–$180k5d Lead a team ensuring the integrity of process validation processes, supporting the transition from development to manufacturing, and ensuring global consistency in validation activities.
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Validation Engineer↗ EllabCounty Louth, Ireland 5d Lead compliant, data-driven qualification and validation activities for autoclaves and steam sterilisation equipment to ensure safe medicine manufacturing.
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Computerized Systems Validation Officer↗ Fresenius Kabi PortugalTondela, Viseu, Portugal 5d Coordinate and oversee Computerized Systems Validation (CSV) activities for GxP-relevant computerized systems in a pharmaceutical environment to ensure compliance and fit-for-purpose use.
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QA Technician – Validation and Qualification (CSV/CQV)↗ ChemoLeón, Castilla and Leon, Spain 5d Ensure compliance of GMP, regulatory, and internal standards; support computerized systems validations and qualifications within a pharmaceutical manufacturing organization.
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MES Platform Engineer↗ SimotechCork, County Cork, Ireland 5d Maintaining and evolving a critical Manufacturing Execution System (MES) landscape within a high-performing pharmaceutical manufacturing environment.
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CQV Consultant↗ Ultimate SolutionsAlcobendas, Community of Madrid, Spain 5d Develop documented evidence to ensure pharmaceutical equipment, processes, facilities, and systems comply with industry quality standards.
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TECNICO DE CUALIFICACIONES Y PROYECTOS↗ Meribel Pharma SolutionsAlcalá de Henares, Community of Madrid, Spain 5d Support pharmaceutical manufacturing operations by managing equipment and facility qualification programs, including calibration, validation protocols, and audits.
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QA Operations Specialist↗ PersonatAmer, Catalonia, Spain 5d Develop and implement validation and qualification policies, strategies, and procedures to ensure the highest quality standards in pharmaceutical manufacturing processes.
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Validierungsingenieur - Medizintechnik / Qualitätssicherung (m/w/d) Workwise GmbHRheinfelden (Baden), BADEN_WUERTTEMBERG 5d Planning, organizing, and accompanying process and test method validations, as well as equipment and tool qualifications.
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Senior Specialist, Engineering Commissioning, Qualification and Validation (CQV) BmsCruiserath - IE 6d Own the qualification of process/utility equipment and validation of computerized systems controlling them, from commissioning/start-up through routine operation, ensuring compliance with regulatory standards.
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IT Business Analyst – PAS|X MES Upgrade (Pharmaceutical Manufacturing) – Contract, AstraZenecaMacquarie Park, New South Wales, Australia 6d Lead local delivery of the PAS|X (Manufacturing Execution System) upgrade at a pharmaceutical manufacturing plant, ensuring system validation and production continuity.
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?CQV Engineer / Senior, Clean Utilities↗ Singapore, S00, SG 6d Qualification and validation of clean utilities (PW/WFI/PS) and clean process gases systems for biopharmaceutical R&D and GMP facilities.
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Validation and Facilities Engineer↗ GalaxypharmaAlbany, NY, US $75k–$100k6d Qualify equipment and cleanrooms, maintain facility systems, and ensure inspection-ready records for a sterile drug production facility.
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Qualification Lead - IT/OT↗ AvaconeIndianapolis, IA, US 6d Lead qualification and quality management for IT/OT systems in GMP-regulated pharmaceutical manufacturing, ensuring compliance with Customer Quality Manuals and regulatory requirements.
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?CQV Engineer / Senior, Facility & Equipment↗ Tanjong Pagar, S00, SG 6d Participate in qualification and validation of factory buildings, temperature control equipment, wet heat sterilization systems, and clean ventilation equipment for biopharmaceutical R&D and GMP facilities.
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Lead I - Engineering Design↗ UstKA, IN 6d Lead CSV Engineer supporting the implementation and validation of Rockwell PharmaSuite MES for GMP production at a pharmaceutical manufacturing site.
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MES Platform Engineer↗ CognizantCork, County Cork, Ireland 6d Configure, build, and validate MES Platform environments (Dev/Test/Production) and manage Computer System Validation (CSV) for pharmaceutical API manufacturing operations.
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Manager, Engineering Computer Systems Validation (CSV)↗ Bristol Myers Squibb UK & IrelandCounty Dublin, Ireland 6d Lead the Computer Systems Validation (CSV) programme for biologics and sterile drug product facilities, ensuring compliance with GxP regulations and data integrity across automated control and enterprise systems.
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Técnico de validación↗ HaysMadrid, Community of Madrid, Spain 6d Lead GMP validation projects for pharmaceutical production and packaging equipment, ensuring compliance with quality standards and regulatory requirements.
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Manager, Senior Engineer Engineering Commissioning, Qualification & Validation↗ Bristol Myers SquibbCounty Dublin, Ireland 6d Lead equipment commissioning, qualification (IQ/OQ/PQ), and requalification activities across Multi-Product Cell Culture and Sterile Drug Product Facility sites to ensure compliance with FDA, EMA, and GMP requirements.
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Lab CSV Engineer↗ Cognizant Life Sciences ManufacturingDublin, County Dublin, Ireland 6d Senior Validation Consultant responsible for Computer System Validation (CSV) of large laboratory systems (LIMS, LES/LabVantage) with a primary focus on validating AI/ML components against emerging regulations like EU GMP Annex 22.
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Process Technician - Fixed-term contract (2 years and 6 months)↗ IntersurgicalWokingham, England, UK 6d Support the development, optimisation, control and validation of manufacturing processes within UK medical device manufacturing.
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Técnico/a Garantía Calidad↗ Mesoestetic Pharma GroupViladecans, Catalonia, Spain 6d Ensuring quality and compliance for a pharmaceutical/cosmetic laboratory through IT system validation, audits, and documentation management.
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QA Validation Specialist↗ Tandem Project Management Ltd.Carlow, County Carlow, Ireland 6d Provide quality oversight for the introduction, commissioning, qualification, and validation of new equipment in a biopharmaceutical manufacturing environment.
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GMP Lab IT & CSV Engineer | Hybrid Cork↗ CatalyxCork, County Cork, Ireland 6d Design, implement, and validate laboratory IT systems within a GMP-regulated pharmaceutical environment to ensure compliance, reliability, and data integrity.
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Project Leader de Transferencias Analíticas (sector farmacéutico) - Indefinido↗ SynthonRemote 6d Lead analytical transfer projects, method validation/verification, and process validation between internal and external laboratories in the pharmaceutical industry.
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Analista de Garantia da Qualidade Júnior – Validação↗ Grupo EmsHortolândia, São Paulo, Brazil 6d Junior Quality Assurance Analyst supporting process execution and monitoring of validation studies to ensure quality, safety, and compliance of production processes.
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Computer System Validation (CSV)↗ Oxford Global Resources 6d Lead Computer System Validation (CSV) activities for GxP-regulated systems to ensure compliant delivery of IT projects in pharmaceutical and life sciences environments.
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Quality Assurance Specialist-Hybrid↗ PSC Biotech® CorporationCarlow, County Carlow, Ireland 6d Provide quality oversight and direction for equipment introduction, validation, commissioning, and qualification activities in a pharmaceutical manufacturing environment.
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Cientifico Asociado - Puebla (Termino Fijo)↗ Johnson & Johnson Innovative MedicineHuejotzingo, Puebla, Mexico 6d Lead and execute high-impact projects, new product introductions, and technology transfers in pharmaceutical manufacturing and validation.
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MES MBR Designer (Siemens Opcenter)↗ Amaris Consulting | Part of MantuSingapore, Singapore 6d Design and validate electronic batch records (MBR) and Process Instructions in Siemens Opcenter Execution Pharma for pharmaceutical manufacturing.
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Senior Validation Specialist↗ Msd IrelandCarlow, County Carlow, Ireland 6d Lead, execute, and oversee filter qualification and validation programs for sterile/aseptic processing, equipment, and processes in a biopharmaceutical manufacturing environment.
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Validation Manager for Holistic Data Management Project | 100% remote | Pharma↗ Ambit IberiaSant Cugat del Vallès, Catalonia, Spain 6d Lead validation activities for a strategic Holistic Data Management (HDM) initiative within a global pharmaceutical environment, ensuring systems meet compliance requirements throughout their lifecycle.
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Senior Product Owner - CSV GskBengaluru Luxor North Tower, IN 6d Lead Computer System Validation (CSV) activities for Manufacturing Execution Systems (MES) to ensure digital systems are compliant, validated, and fit for purpose throughout their lifecycle in a regulated pharmaceutical environment.
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Validation Engineering Specialist II ThermofisherWhitby, Canada $56k–$85k6d Provide specialized validation knowledge and information to support operations and clients, with a main focus on Continuous Process Verification (CPV) for commercial manufacturing of conventional dosage forms.
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