Computer System Validation
328 open positions
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Global Technical Consultant Corporate Accounts - Life Sciences EcolabRemote $129k–$129k1mo Strategic technical partner for corporate clients in the Life Sciences division, bridging technical expertise with client needs to drive innovation, regulatory alignment, and business growth in cleaning, disinfection, and automated bio-decontamination…
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QA Validation Engineer - Manufacturing Systems AbbottNetherlands - Zwolle 1mo Ensure compliance of equipment, processes, and automated systems throughout their lifecycle in a regulated manufacturing environment.
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Associate I, Manufacturing Science & Technology Engineering AlconTuas, Singapore 1mo Validation and qualification activities for highly regulated aseptic manufacturing facilities, ensuring processes remain compliant and in a validated state.
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CSV Analyst ThermofisherBangalore, India 1mo Prepare, execute, and maintain validation deliverables for Microsoft Excel spreadsheet solutions in regulated environments.
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Senior CSV Quality Assurance Specialist (f/m/d) MsdRemote $0k–$0k1mo Lead risk-based Computerized System Validation (CSV) and Data Integrity (DI) for GMP processes, ensuring inspection readiness and compliance with cGMP regulations.
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Lead Engineer, Engineering - Validation LonzaSG - Tuas, Singapore 1mo Lead Validation activities for GMP Biotech manufacturing facility, covering facility, equipment, utilities, and computer systems from URS through PQ.
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QC Validation Engineer GskUSA - Pennsylvania - Marietta 1mo Manages non-testing systems and processes for Quality Control (QC), including new equipment qualification, requalification, and lifecycle management to ensure regulatory compliance.
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Validation Engineer AmgenUS - Rhode Island - West Greenwich 1mo Execute validation activities for manufacturing equipment, support systems, and utilities in a large-scale mammalian cell biotech plant to ensure compliance and product quality.
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Engineer Validation StrykerGurugram, India 1mo Support new product and process introductions, Computer System Validation (CSV), and equipment/process qualifications (IQ/OQ/PQ) for medical device manufacturing systems and digital tools.
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Sr Engineer Computer Systems Validation BristolmyerssquibbDevens - MA - US $99k–$99k1mo Execute computer system validation (CSV) and IT compliance activities for regulated computerized systems in a biologics and cell therapy manufacturing environment.
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QA Engineer VwrHillegom, NLD 1mo Ensure new processes, equipment, and products are introduced in compliance with quality and regulatory requirements for manufacturing expansion.
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Process Engineering Intern EnvistaUnited States of America, California, Yorba Linda 1mo Support equipment programming, qualification (IQ/OQ/PQ), and validation in a regulated manufacturing environment.
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Quality Assurance Validation Engineer↗ Vti Life SciencesThousand Oaks, CA, US 1mo Provide quality oversight for pharmaceutical and biopharmaceutical validation activities, ensuring facilities, systems, equipment, and processes comply with regulatory requirements.
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Senior Quality Engineer, Validation↗ Stemcell TechnologiesBurnaby, BC, CA $95k–$95k1mo Ensure commissioning, qualification, and validation (CQV) strategies and documentation for equipment, facilities, and processes align with regulatory requirements.
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Testovací inžinier pre HMI a PLC (Alarm & Function Testing) (m/ž) SyntegonRemote 1mo Perform Alarm & Function, PLC, and HMI testing for pharmaceutical production lines in compliance with GMP standards.
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CSV Engineer↗ Antaes AsiaSingapore, Singapore 1mo Provide Quality oversight and compliance with GXP standards for computerized systems in Life Science projects.
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Validador de procesos-Manufactura↗ Mega LabelTexcoco, PUE, MX $132k–$132k1mo Ensure processes, materials, equipment, and personnel competencies comply with Quality Management System requirements through validation, monitoring, evaluation, and continuous improvement to guarantee product conformity and customer satisfaction.
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Analista de Validação de Processos e Sistemas Pl - Barueri/SP - Vaga afirmativa para profissionais pretos/pardos e PCD's↗ Daiichi SankyoBarueri, SP, BR 1mo Ensure quality and compliance in pharmaceutical manufacturing through analytical method transfer, computerized system validation, and process/equipment qualification.
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RC-REGULATORY COMPLIANCE-CSV - MES -Manager↗ EYKA, IN 1mo Lead validation and compliance strategy for Manufacturing Execution System (MES) deployments using Werum PAS-X across regulated pharmaceutical systems.
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Data Integrity Specialist↗ Careerwise RecruitmentWaterford, County Waterford, Ireland 1mo Ensuring compliance with regulatory requirements and company policies related to data integrity in a pharmaceutical GMP environment.
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Engineer, Validation↗ Voyant BeautyHolmdel, NJ, US 1mo Lead site validation and contamination control strategy to ensure cGMP compliance for OTC, cosmetics, and regulated systems.
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Químico de Validación sistemas computacionales↗ HP HeptapharmaSan Mateo Atenco, MEX, MX $192k–$192k1mo Validating critical areas, systems, and equipment in a pharmaceutical manufacturing environment to maintain a validated state.
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Senior Clinical Computer System Validation Engineer↗ ICON PlcBlue Bell, PA, US 1mo Ensure compliance with GxP requirements and data integrity principles throughout the lifecycle of computerized systems in a regulated pharmaceutical environment.
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Verification and Validation Engineer↗ Katalyst Healthcares & Life SciencesLittle Rock, AR, US 1mo Mechanical Verification & Validation Engineer supporting medical device product development, design verification/testing, and stability/shelf-life studies.
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Analista Garantia da Qualidade Sênior (Foco em Estéreis) - Aché Pernambuco↗ Aché LaboratóriosCabo de Santo Agostinho, Pernambuco, Brazil 1mo Managing and executing validations for aseptic processes, including sterilizing filtration and radiation sterilization, to ensure process integrity and regulatory compliance in a pharmaceutical manufacturing setting.
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Engineering Compliance and CSV Manager AmbossBerlin 1mo Ensure medical device software is built, verified, and documented to be compliant, trustworthy, and audit-ready; act as an independent evaluator setting standards for 'done and compliant' work.
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CSV Engineer Delta V (Pharma/Biotech)↗ Nusantara Prime Consulting Pte. Ltd.Singapore, S00, SG 1mo Generate CSV Lifecycle documents (VP, Protocols, Summary Reports) for DeltaV processes in biotech/pharma facilities.
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CSV Engineer↗ Orka Lifescience Partners Pte. Ltd.Singapore, S00, SG 1mo Deliver Computer System Validation (CSV) consulting projects for computerized systems in Life Sciences clients, ensuring compliance with GxP and regulatory standards.
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Engineer, QA AstraZenecaQingdao Site 1mo Ensure GMP compliance and operational effectiveness for the pMDI project lifecycle (design, construction, start-up, validation) and Qingdao site QMS establishment.
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Engineer Quality↗ Fedex Supply ChainIndianapolis, IN, US 1mo Technical individual contributor applying engineering principles and data analysis to design, implement, and improve quality processes, controls, and validation activities in regulated environments.
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Validation Specialist↗ Pci Pharma ServicesStamullen, County Meath, Ireland 1mo Implement and execute Process, Facility, and Equipment Validation tasks to ensure client expectations and regulatory compliance (HPRA/FDA) at PCI Pharma Services sites.
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Sr Quality Engineer I↗ Kite PharmaEl Segundo, CA, US $124k–$124k1mo Ensures compliance with cGMP and regulatory requirements for validated computer systems through Computer System Validation (CSV) oversight, risk-based decision making, and quality assurance in a biopharmaceutical manufacturing and laboratory environment.
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Jefe de Validaciones↗ Camber PharmaValle de Cuernavaca, MOR, MX $288k–$288k1mo Leading validation of facilities, equipment, critical systems, manufacturing processes, cleaning, and computerized systems for pharmaceutical production.
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Validation Engineer III↗ Kashiv Biosciences LLC.Piscataway, NJ, US $70k–$70k1mo Develop, test, modify, and create solutions for technical problems within a biopharmaceutical company's validation framework.
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CSV Engineer III↗ ResilienceWest Chester, OH $85k–$85k1mo Independently plan, execute, and lead validation activities for automation and computerized systems in a biomanufacturing environment, ensuring compliance with GxP regulations.
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Validation Engineer II (Medical Industry)↗ Bepc Inc. - Business Excellence Professional ConsultingCiudad Juárez, Chihuahua, Mexico 1mo Develop and execute IQ, OQ, and PQ validation protocols for manufacturing and medical device environments to ensure regulatory compliance.
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Senior Quality Engineer, Validation↗ Advita OrthoGainesville, FL, US 1mo Senior Validation Engineer providing cross-functional support in V&V development, planning, and execution for medical device processes, materials, equipment, and methods.
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Data Center Team Pharmaceutical Project Manager↗ Johnson ControlsIrving, TX, US $115k–$115k1mo 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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