Computer System Validation
589 open positions
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Associate Manager, Engineering - Validation Lonza Group Ltd.Singapore 20d Manage the validation lifecycle program for facility and equipment utilities to ensure compliance with regulatory requirements in pharmaceutical manufacturing.
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Quality Validation Engineer - Equipment Validation NemeraBuffalo Grove, Illinois, us $85k–$105k21d Plan, coordinate, and manage equipment validation projects and supplier quality evaluations to ensure product development and production meet FDA, ISO, and customer quality deliverables.
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Senior Specialist - IT Quality and Computerized Systems Validation BristolmyerssquibbLeiden – NL 21d Provide hands-on support for Computerized System Validation (CSV) and IT Compliance activities for the Leiden Cell Therapy Facility, acting as a Subject Matter Expert for system changes, deviations, and audit readiness.
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Validation Engineer - Equinox↗ MölnlyckeBrunswick, ME, US $104k–$125k21d Lead equipment qualification and process validation for new manufacturing systems and capital expansion projects in a regulated environment.
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Associate Engineer I, Validation↗ Arrowhead PharmaceuticalsMadison, WI, US 21d Entry-level role supporting equipment, utility, analytical instrument, and facility qualification (C&Q) for GMP drug substance manufacturing and testing at a biopharmaceutical manufacturing site.
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Staff Scientist, Molecular Biology↗ Thermo Fisher ScientificTuas, S00, SG 21d Senior technical leader developing and leading system-level Verification & Validation (V&V) strategies for complex life-science products, ensuring product readiness and regulatory compliance.
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Application V&V Engineer (m/f/d) DanaherCHE - Grens - Cytiva, CH 21d Lead verification and validation (V&V) of applications interfacing with multiple subsystems to ensure functional, performance, and integration requirements are met for life sciences and diagnostics products.
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Senior Specialist, Quality Computer Validation (18 month contract) McKessonCAN, ON, Mississauga, CA $99k–$132k21d Lead and support computer system validation and qualification activities for GxP-regulated systems, software, and equipment to ensure compliance with quality management systems and regulatory expectations.
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Senior Specialist - IT Quality and Computerized Systems Validation BmsLeiden – NL 21d Provide subject matter expertise and hands-on support for Computer System Validation (CSV) and IT Compliance activities for the Leiden Cell Therapy Facility.
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Quality Validation Manager IFF (all genders) SanofiFrankfurt am Main, DE €81k–€121k21d Ensure Quality Qualification and Validation activities for a new automated insulin drug substance facility are executed on time and in compliance with regulations.
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Head of Validation - Manufacturing GileadUnited States - California - Foster City $182k–$236k21d Lead the Manufacturing Validation function to establish and execute an integrated, risk-based validation program for a new biologics facility, utilities, equipment, and computerized systems.
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Validation Engineer I↗ American RegentNew Albany, OH, US 21d Develop and execute validation protocols and reports to support the qualification and validation of pharmaceutical manufacturing processes, ensuring facilities, systems, and processes comply with GMPs and perform according to specifications.
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Quality Engineer, Validation↗ STEMCELL TechnologiesBurnaby, British Columbia, Canada $84k–$114k21d Develop metrics for process effectiveness and drive continuous improvement while supporting process, analytical method, and equipment lifecycle verification in cGMP environments.
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Process Engineer↗ EdhikeAthens, GA, US $62k–$73k22d Develop and execute Commissioning, Qualification, and Validation (CQV) documentation and support clients in the Life Sciences industry to manufacture GMP products.
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Principal Automation Engineer – Computer System Validation↗ Eli LillyRichmond, VA, US $68k–$174k22d Design and deliver process automation systems and Computer System Validation (CSV) strategies for a next-generation biotech drug substance manufacturing facility.
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Associate Manager, Engineering - Validation LonzaSG - Tuas, Singapore 22d Manage the validation lifecycle for facility and equipment utilities to ensure compliance with regulatory requirements in pharmaceutical manufacturing.
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Project CQV Engineer, Grey Utilities (12M, Limerick)↗ Careerwise RecruitmentLimerick, County Limerick, Ireland 22d Execute commissioning, qualification, and validation (CQV) activities for grey utilities systems (HVAC, non-process water, compressed air, steam, chilled water) in a Life Sciences facility.
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CQV Engineer (Commissioning, Qualification, and Validation)↗ WuXi AppTecMiddletown, DE, US 22d Execute commissioning, qualification, and validation (CQV) for pharmaceutical manufacturing equipment, facilities, utilities, and automation systems to ensure GMP compliance before production.
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Validation Engineer↗ ElancoElwood, KS, US 22d Coordinate planning and execution of commissioning, qualification, and requalification (C&Q) for facilities, utilities, equipment, and computerized systems at an mAb manufacturing facility.
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Senior IT Quality Compliance Specialist | Pharma | Geel Select ProjectsGeel, Turnhout €42k24d Ensure IT systems, processes, and methodologies remain compliant with GMP guidelines and quality requirements in a pharmaceutical environment.
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Specialist II, Validation↗ ResilienceMississauga, Ontario, Canada $70k–$96k24d Execute validation activities (IQ/OQ/PQ) for clinical and commercial biomanufacturing equipment, utilities, and processes to ensure regulatory compliance and product quality.
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C&Q Execution Lead Engineer↗ Kingsforce Management Services Pte. Ltd.Bukit Merah, S00, SG 25d Lead commissioning and qualification (C&Q/CQV) activities for process and utility systems in pharmaceutical/biotech facilities, ensuring compliance with quality standards and EHS requirements.
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Senior Pharmaceutical Project Manager JciRockville-Virginia-United States of America $95k25d Day-to-day project lead for validated environment and laboratory construction projects (cleanrooms, biosafety cabinets, containment suites) ensuring compliance with IQ/OQ/PQ, data integrity, and regulatory expectations.
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Manager Quality Assurance Validation RegeneronSaratoga Springs, US $92k25d Lead laboratory and analytical equipment validation for a highly automated drug substance manufacturing facility, ensuring regulatory compliance and validated state for commercial and clinical operations.
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Analista de Higiene Eng. Industrial - L'Oréal Operações (São Paulo)↗ L'OréalSão Paulo, Brazil 25d Lead sanitary design validation and CIP/SIP process validation for equipment and systems to ensure hygiene, quality, and industrial engineering standards in the plant.
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Validation Engineer↗ CiqaAñasco, PR, US 25d Execute hands-on validation activities, develop technical documentation, and support site readiness for equipment qualification in a regulated manufacturing facility.
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Automation CSV Engineer – GMP / DeltaV↗ AlgoworksRedmond, WA, US $104k–$146k25d Develop and support lifecycle validation strategies, testing, and technical documentation for GMP automation and computerized systems in regulated manufacturing environments.
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Sr. Engineer, C&Q KenvueNorth America, United States, Pennsylvania, Lititz 25d Senior Engineer leading Commissioning and Qualification (C&Q) activities, ensuring quality, compliance, and validation for manufacturing processes.
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Computerized System Validation (CSV) Site Lead CslAPAC, AU, Broadmeadows, CSL Behring 25d Own and govern Computerized System Validation (CSV) strategy and delivery for Operational Technology (OT) platforms supporting Manufacturing and QC Laboratories.
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Computerized System Validation Specialist RoquetteNewark, US $91k–$121k25d Safeguard patient safety and product quality by ensuring GxP computerized systems remain compliant throughout their lifecycle via risk-based validation practices.
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Expert Compliance et Validation de Systèmes Informatisés F/H MSD FRANCEFrance 26d Expert in Computerized System Validation (CSV) and Compliance for a veterinary pharmaceutical site, ensuring regulatory adherence and data integrity.
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Leader C&Q F/H IMPAC INGENIERIELyon, Rhône 26d Lead C&Q (Computerized & Qualification) strategies for pre-project studies in the pharmaceutical industry, ensuring compliance, timelines, and costs.
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Process Validatie Specialist RomedHoogstraten, Turnhout 26d Prepare, coordinate, execute, and document validation activities for production processes and equipment to ensure compliance with quality standards and regulations.
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Computer System Validation Expert (all gender) AltenRemote 26d Plan, coordinate, and document validation activities for computer-based systems and software solutions according to GAMP5 and GxP requirements.
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CSV Engineer↗ Orka Lifescience Partners Pte. Ltd.Singapore, S00, SG 26d Deliver CSV consulting projects to support implementation of computerized systems (DeltaV, Siemens PCS7, Rockwell PLCs) in Life Sciences clients with compliance of GxP and regulatory standards.
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Validation Engineer III↗ Strive Compounding PharmacyAlachua, FL, US $105k–$115k26d Manage the end-to-end lifecycle of validation documentation and engineering commissioning within a GMP-regulated pharmaceutical facility, serving as a bridge between operational needs and project delivery.
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?Assoc. Director, Quality Assurance Validation↗ King of Prussia, PA, US 26d Lead validation projects for equipment and enterprise systems, ensuring compliance with GxP regulations and industry standards.
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Facilities Engineer IlluminaUS - Wisconsin - Madison $69k26d Develop and execute validation protocols for new or upgraded facilities and utilities supporting medical device manufacturing.
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Commissioning, Qualification, and Validation (CQV) Engineer EurofinsRaleigh, NC, us 26d Commissioning, qualification, and validation (CQV) engineer supporting pharmaceutical and biotechnology clients by writing and executing protocols, performing field verification, and maintaining records for utilities, equipment, and facilities.
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Validation Engineer CaiItalia €45k–€57k26d Develop documentation, write and execute protocols, and generate summary reports for Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.
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Validations Engineer BaxterHuesca, Huesca, ES 27d Validating, commissioning, and optimizing new machines and production processes to ensure quality, safety, and efficiency in pharmaceutical manufacturing.
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CSV Engineer↗ TechtrueupRemote $114k27d Validating Clinical SAS systems and processes to ensure reliable generation of regulatory Tables, Listings, and Figures (TLFs).
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Sterility Assurance Engineer II↗ Merit MedicalTijuana, BCN, MX 27d Develops and executes sterilization validation protocols, manages environmental monitoring for cleanrooms, and ensures compliance with sterility assurance metrics for medical devices.
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Sterility Assurance Engineer II↗ Merit Medical Systems, Inc.Tijuana, Baja California, Mexico 27d Develops and executes sterilization validation protocols and reports for medical devices, ensuring compliance with sterility assurance and environmental metrics in cleanroom settings.
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Senior Computer Systems Validation Engineer↗ 4g ClinicalRemote, US 27d Ensure validation activities and deliverables for core products and study-related projects are properly planned and documented, providing Quality oversight for testing and ensuring validation and data security of infrastructure for 4G study deployments.
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