Computer System Validation
596 open positions
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Validation Analyst, Labs IconChina, Beijing today Ensure the accuracy, reliability, and compliance of laboratory processes and systems supporting clinical trials.
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QA Validation Engineer AbbVieIrvine, CA, us today Execute validation activities for facilities, utilities, equipment, systems, processes, cleaning, and laboratory instruments to maintain a validated state in compliance with cGMP and regulations.
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LabWare CSV Engineer↗ Astrix 1d Develop validation strategies, risk assessments, and documentation for LIMS implementations in GxP-regulated environments.
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Technology Transfer Engineer - Validation Interface↗ Lsc, Life Science ConsultantsCounty Kerry, Ireland 1d Act as the dedicated interface between the Tech Transfer/NPI team and the CQV/Validation function to translate transfer requirements into validation protocols and QRAs.
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CQV Engineer / Qualification & Validation Engineer 80-100% (m/f/d) LonzaCH - Visp 1d Develop and maintain commissioning and qualification documents for new plants, including PQs for critical systems, and support post-implementation SLC in a GMP environment.
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Quality Engineer I, QA Systems BaxterAlliston, Ontario, CA CA$72k–CA$108k1d Lead validation initiatives for manufacturing systems, equipment, and processes to ensure regulatory compliance and data integrity in healthcare manufacturing.
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Lead CSV Engineer↗ PM GroupCork, County Cork, Ireland 1d Lead CSV Engineer responsible for commissioning, qualification, and verification of biotech process equipment and automation systems.
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Técnico/a de Cualificación y Validación (Sector Farmacéutico)↗ Oxigent Technologies €32k1d Execute and review qualification (IQ, OQ, PQ) of pharmaceutical machinery for filling, closing, inspection, and packaging, ensuring GMP compliance and technical excellence in equipment startup.
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Consultor CSV↗ QualipharmaSant Quirze del Vallès, Catalonia, Spain 1d Execute and develop computerized system validation projects (PMV/AR/DQ/IQ/OQ/PQ, data migration) ensuring compliance with internal procedures, regulatory norms, and client requirements.
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Assistant Project Manager RocheSouth San Francisco, US $73k–$135k1d Coordinating Process Validation study documents and supporting Health Authority submissions for critical quality standards.
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VALIDATION ENGINEER FreseniusglobalWilson, NC, US $61k–$86k1d Provides technical support for equipment/system initial validation, requalification, and improvement to ensure compliance with cGMPs in a pharmaceutical plant.
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Process Data Scientist RegeneronRENSS - TECH VALLEY, US $62k–$112k2d Develop and maintain validated tools for automated report generation, data analysis, and KPI tracking to support GMP manufacturing and process controls.
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Analista de Validação de Sistemas e Qualificação de Equipamentos Sênior↗ Phastt - Pharma Services Talent & TechnologySão Paulo, Brazil 2d Senior analyst executing equipment qualification and computerized system validation (CSV) for pharmaceutical manufacturing, packaging, and analytical laboratory systems with GxP impact.
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QA Validation Specialist↗ Thermo Fisher ScientificHorsham, England, UK 3d Lead, coordinate, and perform validation/qualifications for equipment, facilities, systems, cleaning, and computer systems (CSV) at pharmaceutical sites to ensure compliance and a validated state.
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IT Test Validation Engineer↗ Oxford Global ResourcesRemote 3d Design, execute, and validate IT systems and software in a GxP-regulated pharmaceutical environment to ensure compliance and quality.
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Life Science konsult↗ Plantvision ABUppsala, Uppsala County, Sweden 3d Ensuring quality within Life Science through validation, qualification, and commissioning of equipment, systems, and processes for customers.
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Engineering CSV Manager, CQV & Compliance Lead↗ Bristol Myers Squibb UK & IrelandDublin, County Dublin, Ireland 3d Lead the Computerized System Validation (CSV) programme across MPCC and SDPF facilities, ensuring data integrity in a GMP environment.
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Lead/Manager Platform Complaince & Qualification↗ NewPage SolutionsRemote 3d Execution engine for a shared compliance service supporting a pharmaceutical company's Platform Engineering organization, ensuring platforms are qualified, evidenced, and inspection-ready.
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Analista da Garantia de Qualidade Sênior (Validação)↗ EmsHortolândia, São Paulo, Brazil 4d Senior Quality Assurance Analyst specializing in validation studies, analytical method development, and regulatory compliance within the pharmaceutical industry.
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Senior Validation Manager↗ Ambit IberiaBarcelona, Catalonia, Spain 4d Lead the validation strategy for the Medicine Data Foundation (MDF), a next-generation data platform enabling data-driven decision-making in the pharmaceutical domain, specifically supporting the Risk-Based Quality Management (RBQM) initiative.
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Associate Validation & Qualification PfizerIndia - Vizag 4d Support Technology Transfer activities, execution of validation batches, and ensure compliance with regulatory requirements for safe and effective products.
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Quality Management Engineer - Schwerpunkt Validierungsmanagement (m/w/d) SCHÖLLY FIBEROPTIC GMBHRemote 4d Define and continuously develop validation management guidelines (qualification, processes, computer systems, test methods) and ensure, verify, and release validation activities and documents for development and production.
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Engineer I - Engineering, Validation CatalentMadison, WI, US 4d Support quality assurance and validation activities to ensure compliance with regulatory and internal quality standards in biologics manufacturing.
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GMP Lab IT & CSV Engineer — Hybrid Role↗ CatalyxCork, County Cork, Ireland 4d Ensuring compliance, reliability, and data integrity of laboratory IT systems within a GMP-regulated pharmaceutical environment.
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QA CSV Specialist↗ R&d PartnersTipperary, County Tipperary, Ireland 4d Validating Laboratory Information Management Systems (LIMS), analytical lab equipment, and computerized systems in a regulated pharmaceutical environment to ensure data integrity and compliance.
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QA Validation Lead↗ Robotics TechnologiesTampa, FL, US 4d Lead validation qualification activities for OT and IT systems in trading environments, ensuring compliance with Quality Manuals and regulatory requirements.
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Instrument Qualification Engineer↗ Cognizant Life Sciences ManufacturingCork, County Cork, Ireland 4d Execute Laboratory Computer System Validation activities and deliver validation elements for lab systems within the Analytical Instrument Qualification (AIQ) framework.
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QA Validation Records Specialist↗ AccproDundalk, County Louth, Ireland 4d Reconcile, organize, and digitize archived validation documentation while implementing a new electronic archival system and electronic True Copy process for a pharmaceutical organization.
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Qualitätssicherungsmitarbeiter Sterility Assurance (Mediafill) - befristet (m/w/d)↗ Vetter PharmaRavensburg, Baden-Württemberg, Germany 4d Responsible for creating, reviewing, and approving GMP-relevant validation documents for aseptic process validation, conducting on-site observations of aseptic processes, and optimizing processes based on scientific risk analyses.
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Quality Assurance Specialist↗ eTeamDundalk, County Louth, Ireland 4d Reconcile, organize, and digitize archived validation documentation while implementing a new archival system and electronic True Copy process.
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?Project Engineer↗ Hopkinton, MA, US 4d Execute engineering support for procurement, enrollment, installation, validation, and commissioning of equipment and systems in a biotech/pharmaceutical manufacturing environment.
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Analista de Garantia da Qualidade↗ Phibro Saúde Animal BrasilGuarulhos, São Paulo, Brazil 4d Ensuring equipment, processes, and computerized systems meet quality and regulatory standards for animal health and nutrition products.
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CSV Validation Analyst↗ ZifoMexico City, Mexico 4d Execute computer system validation (CSV) activities, support lab equipment and applications, and ensure data integrity and compliance in GMP laboratory and manufacturing environments.
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Associate Validation Engineer – GDP Customer Qualification and Distribution Validation↗ Biomarin Pharmaceutical Inc.Cork, County Cork, Ireland 4d Execute documented bona fide and technical capability assessments to qualify and approve customers and distribution partners for receiving, storing, and distributing BioMarin medicinal products.
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CQV / Validation / Process Engineering - Aerospace↗ Capgemini EngineeringVila Nova de Gaia, Porto, Portugal 4d Support commissioning, qualification, validation, and process engineering activities within regulated environments for aerospace and life sciences projects.
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Consultant - Business Consulting Risk - TMT - CNS - RISK - DIGITAL RISK - Mumbai↗ EYMumbai, Maharashtra, India 4d Consultant performing Computer System Validation (CSV) assessments for Life Sciences clients to ensure compliance with internal procedures, leading practices, and regulatory requirements.
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Konsulter inom processteknik och validering till vårt konsultnätverk↗ Dedicare Life ScienceRemote 4d Consultant for process engineering and validation/qualification projects in the Life Science industry.
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GMP Lab Analyst | CSV Consultant↗ RephineBarcelona, Catalonia, Spain 4d GMP Lab Analyst transitioning to CSV Consultant, applying pharmaceutical laboratory knowledge to validate computerised systems in regulated environments.
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IT Support Engineer (MES)↗ CognizantCork, County Cork, Ireland 4d Software engineer providing IT support, system maintenance, and validation for pharmaceutical manufacturing systems in a customer site.
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Quality Assurance- Executive↗ Glenmark PharmaceuticalsNashik, Maharashtra, India 4d Prepare protocols and reports for process validation, cleaning validation, packing validation, and hold time studies; coordinate cross-functional execution; track batches; and perform continuous process verification.
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Ingeniero/a de Validación de Procesos – Pharma & Equipos Industriales↗ BETWEEN GroupTerrassa, Catalonia, Spain 4d Design and execute validation protocols for industrial equipment and processes in highly regulated industries (pharma, biotech) ensuring compliance with GMP standards.
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Validation Engineer↗ Nacs, Inc.Ham Lake, MN, US $90k–$105k4d Design, implement, and manage equipment validation and asset lifecycle programs for facilities, equipment, instruments, systems, and software in regulated environments.
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Process Engineer II, Manufacturing Process Validation & Equipment Qualification↗ LantheusSpringfield, NJ, US $89k–$148k4d Process Engineer II responsible for planning, executing, and maintaining validation activities for pharmaceutical and radiopharmaceutical manufacturing operations, ensuring processes and equipment remain in a validated state.
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