Computer System Validation
590 open positions
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CQV Tech Lead – Commissioning, Qualification & Validation – Life Science↗ PQE Group 27d Lead and support Commissioning, Qualification & Validation (CQV) activities for HVAC systems, clean utilities, and manufacturing equipment in pharmaceutical and life science projects.
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Systems, Engineer IV - eQMS DD&T↗ Takeda PharmaceuticalsKA, IN 27d Lead the end-to-end lifecycle of the eQMS (electronic Quality Management System) product, including strategy, roadmap, development, and global technical support for GxP environments.
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Ingénieur stérilisation autoclaves F/H FortilCany-Barville, Dieppe 28d Specialized role in sterilization and autoclave processes for industrial projects, particularly in pharmaceutical or medical device environments.
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CDI - Coordinateur Qualification / validation (F/H) ValdepharmVal-de-Reuil, Les Andelys 28d Coordinateur Qualification / validation responsible for writing qualification documentation, risk analyses, and validation plans for pharmaceutical manufacturing processes.
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Senior Manager, ECQ Delivery BmsSummit West - NJ - US 28d Senior Manager leading Equipment Commissioning & Qualification (ECQ) teams to validate pharmaceutical manufacturing and laboratory equipment, facilities, and computerized systems in compliance with cGMP and GXP regulations.
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Validation Engineer↗ Boxx Technologies, Inc.Austin, TX, US 28d Lead the development, execution, and documentation of validation protocols to ensure production processes and equipment meet quality standards and regulatory requirements.
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Validation Engineer – Medical Device Manufacturing↗ JobsrusAñasco, PR, US $58k28d Execute process validation (IQ/OQ/PQ) and support NPI/NPD for medical device components, ensuring compliance with FDA and ISO standards.
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Associate Validation - ARTIST AmgenIndia - Hyderabad 28d Execute validation activities for data platforms and software applications to ensure compliance with standards and support engineering deployment.
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Validation Engineer↗ Boxx TechnologiesAustin, TX, US $96k28d Lead the development, execution, and documentation of validation protocols to ensure production processes and equipment meet quality standards and regulatory requirements.
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Associate Validation Engineer SoterahealthSomercotes, GB 28d Support planning, coordination, and execution of validation activities for customer, facility, and research projects in a highly regulated sterilization environment.
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CSV Engineer↗ Cognizant Life Sciences ManufacturingCork, County Cork, Ireland 28d Validate lab systems and instruments in QCL Labs and Manufacturing Operations to ensure compliance with GMP guidelines and 21CFR Part 11.
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Plant Process Commissioning Qualification Engineer↗ SanofiSwiftwater, PA, US 28d Ensure quality and compliance of engineering documentation for commissioning and qualification of packaging, inspection, and drug substance processing systems in vaccine and pharmaceutical manufacturing.
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Associate Engagement Manager (GxP Validation Expert)↗ QuantiphiMH, IN 29d Lead and execute GxP validation activities for cloud platforms, virtualized environments, and network components in regulated industries.
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Lab Computer System Validation Engineer↗ Katalyst Healthcares & Life SciencesWarsaw, IN, US 29d Execute laboratory Computer System Validation (CSV) activities to ensure validation and ongoing compliance of laboratory instruments and systems.
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Validation Manager ThermofisherAllentown, Pennsylvania, USA 29d Manage validation activities to ensure product quality and regulatory compliance in pharmaceutical/biotech manufacturing.
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JT041 - MANUFACTURING ENGINEER↗ Quality Consulting GroupJuncos, PR, US 29d Production support engineering for testing methods, procedures, and problems in manufacturing operations.
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QA Validation Specialist↗ Dps Group GlobalCounty Kerry, Ireland 29d QA Validation Specialist responsible for GxP validation governance, compliance, and documentation approval in an industrial/pharmaceutical setting.
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Validation Project and Engagement Manager↗ Jc AutomationPR, BR 29d Plan, lead, and control the delivery of validation, qualification, and procedural documentation services for the expansion of a validated LabWare LIMS supporting GMP Quality Control laboratory operations.
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CQV Ingenieur / Qualifizierungs- und Validierungsspezialist 80-100% (m/w/d) LonzaCH - Visp 29d Responsible for qualification and validation of process engineering equipment and facilities, ensuring compliance and optimizing processes.
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Manager, GxP Systems ModernaTXWarsaw - Poland 1mo Lead validation, qualification, and testing activities for GxP applications and infrastructure across Moderna's Digital landscape using Computer Software Assurance (CSA) principles.
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CSV Engineer↗ Integrix Solutions Pte. Ltd.Singapore, S00, SG 1mo Lead Computer System Validation (CSV) for Windows OS upgrades and administer WinCC/Siemens PLC systems in regulated life science environments.
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Director - Computer Systems Validation VeevaRemote $150k1mo Director of Computer Systems Validation Program providing oversight of validation teams to ensure on-time, on-budget delivery of CSV activities for Veeva Vault technology in the life sciences industry.
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Analista de Validação de Sistemas Computadorizados SR (Qualidade)↗ Unither PharmaceuticalsSão Paulo, São Paulo, Brazil 1mo Responsible for the validation of computerized systems and their lifecycle, ensuring compliance with quality manuals and regulatory norms in a sterile pharmaceutical manufacturing environment.
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CQV Engineer - SIP/Thermal Mapping↗ PM GroupDublin, County Dublin, Ireland 1mo Senior CQV/Thermal Validation Engineer responsible for SIP cycle development, Ellab thermal mapping, and Performance Qualification of GMP process equipment.
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Engineer, Computer Software Assurance↗ MasimoRemote 1mo Ensuring computerized systems used in GxP processes comply with global regulatory requirements (FDA, ISO) and providing strategic oversight of CSV activities.
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Quality Test Engineer↗ BdFranklin Lakes, NJ, US 1mo Plans, performs, and leads lab validation activities for new/improved lab concepts, technologies, and equipment to support product development and commercial robustness.
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Validation Specialist↗ NouryonLos Reyes Acaquilpan, México, Mexico 1mo Ensure processes, equipment, computerized systems, facilities, and critical utilities used in pharmaceutical manufacturing, testing, storage, and distribution are properly qualified and validated for GMP compliance.
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Engineer, Computer Software Assurance DanaherRemote 1mo Ensuring computerized systems used in GxP processes comply with global regulatory requirements and providing strategic oversight of CSV activities.
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Validation Engineer I ElevateBioElevateBio $105k1mo Perform qualification activities (IQ, OQ, PQ) for manufacturing facilities, utilities, equipment, and instruments in cGMP environments.
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Qualification Engineer PfizerIndonesia - Jakarta 1mo Plan, coordinate, execute, and document commissioning, qualification, and requalification activities for manufacturing equipment, utilities, facilities, HVAC, cleanrooms, and environmental-control systems to ensure compliance and safety.
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GxP Systems and Support Administrator CaiUSA 1mo Lifecycle administration of GxP and Quality governed systems (eQMS, CMMS, Digital Validation) within a professional services firm.
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MX/ LS CSV Consultant - Business Consulting InfosysMéxico 1mo Consultant specializing in IT Computerized System Validation (CSV) for Life Sciences, ensuring compliance in system development and release cycles.
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QA Officer Validation SharpHamont-Achel, Maaseik 1mo Develop, implement, maintain, and monitor validation policies for systems, processes, installations, and equipment in compliance with GMP guidelines and pharmaceutical regulations.
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Valideringsledare (Life Science)↗ Capgemini EngineeringStockholm, Stockholm County, Sweden 1mo Lead validation and qualification activities for equipment, instruments, and processes in the Life Science industry, ensuring compliance with regulatory requirements.
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Senior Engineer, Validation AbbVieCincinnati, OH, us 1mo Lead maintenance, engineering, and validation activities for clinical packaging equipment, facilities, and utilities to ensure product quality and regulatory compliance.
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Validation Lead↗ Astellas PharmaTralee, County Kerry, Ireland 1mo Lead daily operations of the Validation function to ensure facilities, utilities, equipment, computerized systems, manufacturing processes, and aseptic operations perform as intended and reliably produce safe, effective, and compliant biopharmaceutical…
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Director, Digital Quality GMP Computer Oversight GileadUnited States - Maryland - Frederick 1mo Develop and oversee risk-based validation and assurance strategies for GxP computerized systems to ensure patient safety, product quality, and regulatory compliance.
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Validering MedTech/Pharma till QRIOS Life Science & Engineering, Malmö↗ QriosMalmo, Skåne County, Sweden 1mo Validating equipment, processes, methods, and systems for MedTech and Pharma clients according to regulations like ISO 13485, MDR, GMP, and GAMP5.
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Quality & Compliance Manager, Computer System Validation PrecisionmedicinegroupRemote (US) 1mo Manage quality oversight and lifecycle validation of GxP computerized systems supporting CRO and laboratory operations to ensure data integrity and regulatory compliance.
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Analytical Method Validation Specialist EurofinsWavre, Wallonia, be 1mo Coordinate and implement analytical method validation activities to support Quality Control operations in a pharmaceutical setting, ensuring compliance with GMP requirements.
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