Computer System Validation
595 open positions
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Senior CQV Engineer↗ Jacobs 1mo Leading commissioning, qualification, and validation (CQV) of equipment, systems, and processes for drug substance/product manufacturing, sterile facilities, and utilities.
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Commissioning & Qualification Engineer↗ Careerwise RecruitmentWaterford, County Waterford, Ireland 1mo Commissioning and Qualification Engineer for laboratory systems, autoclaves, and clean utilities in GMP-regulated pharmaceutical environments.
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【今市】生産技術（MSAT Execution） GskJapan - Tochigi - Imaichi 1mo Subject matter expert validating, optimizing, and maintaining robust manufacturing and cleaning processes to ensure consistent production of safe, effective, and cost-efficient pharmaceutical products.
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Senior Commissioning Qualification Validation Engineer PSC BiotechMelbourne, Victoria 1mo Lead Commissioning, Qualification, and Validation (CQV) functions to ensure systems, facilities, and equipment meet design requirements for biomedical and pharmaceutical projects.
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Data Validation and Support Specialist BioAgilytixMelbourne, Victoria 1mo Provide IT and application support for scientific applications and perform Computer Systems Validation (CSV) activities, including spreadsheet validation, to ensure compliance with regulatory guidelines in a clinical research environment.
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CIP Engineer (Clean-in-Place) - Engineering & CQV↗ Hyde Engineering + ConsultingTuas, West Region, Singapore 1mo Design, commission, qualify, and validate Clean-in-Place (CIP) systems for pharmaceutical and biopharmaceutical manufacturing facilities to ensure compliance with cGMP and regulatory standards.
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Spécialiste des systèmes de qualité/Quality Systems Specialist↗ Fresenius Medical CareVaudreuil-Dorion, Quebec, Canada 1mo Ensures quality and compliance for manufacturing processes, new product designs, and existing products in a pharmaceutical/medical device facility.
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CSV Junior Consultant (pharma) (^)↗ BETWEEN GroupMadrid, Community of Madrid, Spain 1mo Junior CSV Consultant validating computerized systems in regulated pharmaceutical environments.
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Senior Specialist, Validation Engineer II BristolmyerssquibbDevens - MA - US $93k1mo Qualifies and validates manufacturing, laboratory equipment, facilities, and utilities to ensure they remain in a qualified state for biologics/cell therapy production.
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QC Cleaning Validation Specialist↗ Astellas PharmaTralee, County Kerry, Ireland 1mo Provide technical and quality oversight for cleaning validation activities to ensure equipment, facilities, and manufacturing processes meet regulatory and quality requirements.
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Senior Specialist, Validation Engineer II BmsDevens - MA - US $93k–$112k1mo Qualifies and validates manufacturing equipment, facilities, utilities, and computer systems for biologics/cell therapy production to ensure compliance with cGMP and regulatory standards.
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Validation Engineer Sterilization (MS&T) GaldermaUppsala 1mo Subject matter expert for sterilization processes, specifically leading validation and qualification of autoclaves and VHP decontamination systems to ensure compliance and patient safety.
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Quality Engineer↗ Urgo Medical North America LLCFort Worth, TX, US $105k1mo Develop, execute, and maintain quality protocols and validation activities for medical device manufacturing systems and processes.
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Sr Business Systems Analyst DexcomPenang, Malaysia 2mo Subject Matter Expert for validation and compliance of Enterprise and Manufacturing Systems (MES, ERP, QMS, SCADA, PLC) in a medical device environment.
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Superviseur(e) - Validation (Qualité)↗ Church & Dwight Co., Inc.Montreal, Quebec, Canada 2mo Supervising all operational validation activities, planning/scheduling, and reviewing validation programs for a pharmaceutical manufacturing plant.
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Specialist, Validation Roechling Medical Solutions SENeuhaus am Rennweg, THUERINGEN 2mo Planning and execution of qualification and validation measures for medical devices, systems, software, and processes in compliance with GMP and regulatory standards.
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Process Validation Manager↗ GrifolsDublin, County Dublin, Ireland 2mo Manage process validation staff and consultants to deliver new process validation, technical transfer, and equipment qualification projects in aseptic manufacturing environments.
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Computer Systems Validation Intern DanaherFargo, North Dakota, United States 2mo Intern gaining hands-on experience in regulated industry operations alongside validation engineers and software developers.
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Ingenieur I Naturwissenschaftler I Techniker (m|w|d) für den Bereich Qualität und Validierung EurofinsCalw, BW, de 2mo Validating processes and assessing development results for cleaning, packaging, and sterilization in a sterile packaging environment.
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Engineer II, Computer Systems Validation ThermofisherGreenville, North Carolina, USA 2mo Support validation activities for automation systems, manufacturing equipment, and computerized systems to ensure compliance and operational readiness.
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Computer System Validation Expert (all gender) ALTEN GmbH MünchenMannheim, BADEN_WUERTTEMBERG 2mo Plan, execute, and document computer system validation activities ensuring regulatory compliance for pharmaceutical industry systems.
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Senior Quality Engineering Specialist PrimemedicineCambridge $111k2mo Provides hands-on operational support for GxP software, equipment, calibration, preventive maintenance, and vendor oversight to ensure systems and equipment remain compliant and inspection-ready.
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Staff Quality Engineer, Microbiology and Sterilization StrykerIrvine, California $96k2mo Lead sterilization process development, validation, and requalification while ensuring microbiological control and biocompatibility compliance across the product lifecycle.
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Expert (m/w/d) Sterility Assurance – Sterilization Validation Simtra Deutschland GmbHHalle (Westfalen), NORDRHEIN_WESTFALEN 2mo Responsible for fulfilling regulatory requirements for the validation of sterilization and decontamination processes at the Halle/Westfalen site, representing the department in internal and customer projects.
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QA Validation Engineer↗ CaiLimerick, County Limerick, Ireland 2mo Execute IQ, OQ, and PQ activities for GMP equipment and systems in pharmaceutical and biotechnology facilities.
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Validation Engineer FreseniusglobalMelrose Park, IL $65k2mo Execute equipment, system, and process validation studies (IQ/OQ/PQ) and requalifications in a cGMP regulated manufacturing environment to ensure compliance and performance.
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CQV Engineering Roles - Senior / Lead / Manager - Opportunities 2026↗ PM GroupDublin, County Dublin, Ireland 2mo Senior/Lead/Manager CQV Engineer responsible for Commissioning, Qualification, and Validation of Upstream, Downstream, Syringe line, and E-beam systems for life sciences and pharmaceutical projects.
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Engineers in Life Science↗ AltenUppsala, Uppsala County, Sweden 2mo Experienced consultants for automation, validation, and process development projects in GMP-regulated Life Science environments.
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Computer Systems Validation Specialist III LonzaUS - Portsmouth, NH 2mo Leads teams in assessing new and changing computer systems to ensure compliance with company policies and industry guidance, acting as the QA CSV representative for projects.
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Sr. QA Computer System Validation Mgr. 4dmoleculartherapeuticsHybrid $126k2mo Overseeing validation, compliance, and lifecycle management of GxP computer systems (clinical, quality, lab, enterprise, manufacturing) to ensure regulatory adherence and support business objectives.
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