Computer System Validation
601 open positions
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Senior Validation Engineer PfizerUnited States - Kansas - McPherson $83k–$138k8d Lead complex validation projects and ensure compliance with cGMPs and GxP guidelines for sterile products and medical devices.
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Valideringsingenjör Life Science↗ Knightec GroupMalmo, Skåne County, Sweden 8d Validating processes, equipment, and computerized systems to ensure safety and quality for Life Science customers.
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CSV Engineer↗ Coalesce Management ConsultingSingapore, Singapore 8d Lead CSV activities for equipment and computerised systems in a GMP-regulated biopharmaceutical facility, supporting migration and validation programmes.
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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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Software Validation Engineer (LIMS-Windchill)↗ Bepc Inc. - Business Excellence Professional ConsultingCiudad Juárez, Chihuahua, Mexico 8d Administer Windchill change management and support LabVantage LIMS implementation in a regulated Life Science environment.
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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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Spécialiste, Validation / Specialist, Validation↗ Jubilant Pharma LimitedMontreal, Quebec, Canada 10d Develop and execute qualification protocols for equipment, computerized systems, utilities, and manufacturing operations in sterile pharmaceutical environments.
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MES LCM / CSV Engineer RETEL Neuhausen AGNeuhausen am Rheinfall, Schaffhausen 11d Managing the lifecycle, optimization, and validation of MES systems (WERUM PAS-X) and leading Computer System Validation (CSV) projects in regulated environments.
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Consultant CSV und Laborinformatik (m/w/d) DatalynxBirsfelden, Arlesheim 11d Implementing technical and procedural adjustments for computerized systems in laboratory and production based on compliance gap analyses for Data Integrity and Annex 11.
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Process Technician - Fixed-term contract (2 years and 6 months)↗ Intersurgical UKHill Head, England, UK 11d Support the development, optimisation, control and validation of manufacturing processes within UK medical device manufacturing.
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System Validation Specialist (M/F)↗ Tecnimede GroupSintra, Lisbon, Portugal 11d Setup and maintain CSV validation platforms to ensure software stack compliance with cGMP guidelines and internal practices for drug product lifecycle.
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Manager, Validation Engineering↗ STEMCELL TechnologiesBurnaby, British Columbia, Canada $117k–$175k11d Lead a team of quality validation engineers to oversee Quality Assurance Validation strategies, ensure regulatory compliance, and drive engineering excellence in a biotechnology company.
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Spécialiste validation↗ Laboratoire Riva IncBlainville, Quebec, Canada 11d Plan, write, coordinate, execute, and follow up on qualification and validation activities for manufacturing processes, cleaning processes, equipment, and utility systems.
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Process Technician - Fixed-term contract (2 years and 6 months)↗ Intersurgical PortugalHill Head, England, UK 11d Support the development, optimisation, control and validation of manufacturing processes within UK medical device manufacturing.
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Business System Validation Senior Specialist MsdPOL - Mazowieckie Wojewodztwo - Warsaw (Trade Center), PL 11d Lead enterprise-wide validation strategies for data integration and automation solutions supporting clinical and business operations, ensuring regulatory compliance and inspection readiness.
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Validation Engineer BarrywehmillerIndianapolis, IN, US 11d Develop and execute validation and FDA compliance documents/protocols for pharmaceutical equipment and processes, including Process Equipment, Facility/Utilities, and Cleaning/Process.
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Analista de validaciones↗ Servicios Profesionales 11d Validations analyst for a pharmaceutical laboratory, ensuring compliance with regulatory standards for sterile and non-sterile medications.
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TECNICO AREA CALIDAD Y VALIDACIONES↗ Qualing Argentina S.R.L.Buenos Aires, Buenos Aires Province, Argentina 11d Calibrating equipment and systems for the pharmaceutical industry to ensure medication quality.
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Validation Engineer↗ Barry Wehmiller Companies IncIndianapolis, IN, US 11d Develop and execute validation and FDA compliance protocols for pharmaceutical equipment and processes, including risk assessments and qualification data analysis.
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QA Validation Manager↗ Lnk InternationalHauppauge, NY, US 11d Leads QA input and oversight for validation projects supporting commercial manufacturing of solid and liquid oral dose OTC products, ensuring compliance with FDA regulations and company policies.
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Quality Manager (CSV)↗ B. Braun GroupBarcelona, Catalonia, Spain €50k11d Develop, maintain, and improve processes, templates, and guidance for qualification and validation of computerized systems in accordance with GAMP 5 and internal requirements.
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Analista de Validaciones / Laboratorio Oticoff↗ Laboratorios EcarMedellín, Antioquia, Colombia 11d Support validation and qualification activities for processes, equipment, systems, and facilities to ensure compliance with GMP, regulatory requirements, and quality standards for sterile product manufacturing.
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Senior Specialist, QC Support, Cell Therapy BmsDevens - MA - US $91k–$110k11d Manage the lifecycle activities of QC laboratory equipment, including validation, qualification, maintenance, and troubleshooting to support GMP-compliant operations.
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CQV Consultant↗ PQE GroupBarcelona, Catalonia, Spain €30k11d Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems in production facilities.
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Quality Engineer med inriktning mot validering↗ Agap2 SwedenUppsala, Uppsala County, Sweden 11d Validating and qualifying sterilization processes in autoclaves to ensure microbiological quality and sterility assurance.
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Staff Validation Engineer ThermofisherGreenville, North Carolina, USA 11d Lead validation activities for critical systems, equipment, and processes enabling the development and manufacturing of therapies in a GMP environment.
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PSS Analytical Instrument Qualification Specialist EurofinsRingaskiddy, CO, ie 12d Planning and execution of Analytical Instrument Qualification (AIQ) activities for In-Process Technology (IPT) equipment within manufacturing areas to ensure GMP compliance.
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C&Q Consultant for Pharma Industry SyntegonBarcarena, Lisboa, pt 12d Commissioning and Qualification Consultant supporting Life Science companies in Portugal to ensure GMP compliance and equipment validation.
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Lab Automation Project Engineer↗ Informatech Consulting, Inc.Lansdale, PA, US $125k–$146k12d Designing, configuring, and validating pharmaceutical manufacturing automation and laboratory systems to ensure compliance with GXP and 21 CFR Part 11.
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Qualification Engineer Pharma (m/w/d) NES Global Deutschland GmbHKonstanz, BADEN_WUERTTEMBERG 12d Planning, executing, and managing qualification activities for process equipment and utility systems in a pharmaceutical production environment.
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GCP & Computer System Validation Auditor↗ Biorasi 12d Plans, conducts, and documents GCP audits and computerized system validation activities to ensure compliance with regulatory requirements and quality standards in clinical research.
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Analista de Validación↗ Neolpharma Sa de CvCoyoacán, Mexico City, Mexico 12d Validating facilities, systems, equipment, processes, cleaning, and maintenance in an injectable drug manufacturing plant.
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Validation Engineer FerringMinneapolis, Minnesota, United States $77k–$110k12d Prepare, review, and execute commissioning, qualification, and validation documents for processes, materials, equipment, cleaning, and computerized systems/software in a cGMP regulated manufacturing environment.
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PSS Analytical Instrument Qualification Specialist↗ Eurofins Pss Insourcing SolutionsRingaskiddy, County Cork, Ireland 12d Planning and execution of Analytical Instrument Qualification (AIQ) activities for In-Process Technology (IPT) equipment within manufacturing areas to ensure compliance with GMP requirements.
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Quality Manager Design & Qualification (all genders) - limited until 30.06.2028 SanofiFrankfurt am Main, DE €81k–€108k12d Ensure Commissioning and Qualification (C&Q) activities for a new insulin drug substance facility, covering design, utilities, equipment, and computerized systems.
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R&D Validation Engineer↗ Validation & Engineering Group, IncDorado, PR, US 12d Develop and execute equipment validation protocols (IQ/TQF), design tools/fixtures, and support process development to ensure compliance and scalable operations in regulated life sciences.
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Engineer I, Production↗ GetingeWayne, NJ, US $88k–$92k12d Review production documentation, address deficiencies, perform equipment qualifications, and lead process validation requirements to ensure compliance.
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Documentation Engineer↗ Acg WorldMumbai, Maharashtra, India 12d Creating and reviewing Master Validation Documents (FS, HSD, SDS, HDTR, SDTR, I/O, ITR, FAT, IQ, OQ) for pharma manufacturing and heavy machinery.
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