Computer System Validation
302 open positions
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Assoc. Dir , Technology Compliance MsdIRL - Meath - Dunboyne, IE 7d Lead site functional and cross-functional structures for computerized system validation (CSV) and IT/OT compliance in biologics drug substance manufacturing.
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Senior Manufacturing System Engineer StrykerBelfast, United Kingdom $37k–$37k7d Own and validate digital systems supporting medical device manufacturing operations, ensuring compliance with GMP, FDA, and ISO standards.
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Quality Assurance & Quality Control (Multiple Roles and Locations) Industrial Placement, 2027 GskUK - West Sussex - Worthing $26k–$26k7d Industrial placement roles in Quality Assurance & Quality Control supporting drug product lifecycle, equipment qualification, and digital quality systems within a regulated healthcare environment.
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Validation Engineering Co-op ThermofisherMississauga, Canada $0k–$0k7d Execute and prepare validation protocols (IQ, OQ, PQ) for equipment and facilities systems, maintain documentation, and support Quality Operations and Process Technology.
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Analista de Validação de Equipamentos - Pleno - Itapecerica da Serra↗ BrainfarmaItapecerica da Serra, SP, BR 7d Ensuring equipment validation compliance and managing qualification protocols for pharmaceutical manufacturing and packaging equipment.
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Sr. Computer System Validation Engineer↗ Takeda PharmaceuticalsCuajimalpa, DIF, MX 7d Develop and oversee validation documentation, lead validation planning and execution for IT platforms and infrastructure, and ensure compliance with regulatory standards.
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Validation Supervisor, Technical Operations - Self Care (FIXED TERM- 12 MONTHS) KenvueLatin America, Brazil, Sao Paulo, Sao Jose dos Campos 7d Lead validation programs for manufacturing, packaging, and cleaning of pharmaceutical products (liquids, solids, semi-solids) to ensure compliance and operational efficiency.
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VALIDATION ENGINEER↗ Formulated SolutionsLargo, FL, US 7d Own system validation activities, specifically leading the transition from paper to electronic batch records (eBR) and managing validation for other systems/equipment.
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Senior Support Specialist- Lab Operations AbbVieNorth Chicago, IL, us 7d Plans and executes validation activities, manages purchasing requisitions, and supports the implementation of QC Laboratories' validation programs to ensure timely delivery of goods and services.
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Técnico PPLM (Product & Process Lifecycle) GsknchAlcalá de Henares, Madrid $45k–$61k8d Lead Product & Process Lifecycle Management for products manufactured on site, ensuring validated processes and compliance with health authority standards.
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Technical Project Engineer AbbottIreland - Donegal Town 8d Develop and conduct project plans and validations to support manufacturing product performance and yields for blood glucose test strips and sensors.
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Computer System Validation Engineer CaiMilano, Provincia di Milano $34k–$34k8d Develop and execute Computer System Validation (CSV) protocols and test scripts for Life Sciences and Mission Critical industries, ensuring compliance with GxP and 21 CFR Part 11.
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Engineer, Computer System Validation↗ Hoya Medical Singapore Pte. Ltd.Clementi, S00, SG 10d Ensures engineering compliance with international regulations (FDA 21 CFR Part 11, EUMDR, MDSAP) for GxP-regulated computerized systems across Hoya Surgical Optics globally.
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EQUIPMENT VALIDATION ENGINEER↗ Anter Consulting Pte. Ltd.Singapore, S00, SG 11d Author and execute IQ/OQ/PQ protocols and Computer System Validation (CSV) for Repligen KrosFlo tangential flow filtration (TFF) systems in a GMP biologics facility.
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QA Systems Engineer BaxterMedina, New York $76k–$76k11d Execute complex validations (IQ, OQ, PQ, MSA) for processes, equipment, and computerized systems within a regulated manufacturing facility.
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Senior Commissioning Qualification Validation Engineer PSC BiotechMelbourne, Victoria 12d 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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Associate Director, Computer Systems Assurance (Quality) NurixBrisbane, Queensland 12d Own and advance the Computer Systems Assurance (CSA) program for GxP-regulated SaaS and cloud-hosted platforms in a clinical-stage biopharmaceutical company.
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Data Validation and Support Specialist BioAgilytixMelbourne, Victoria 12d 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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Senior Commissioning and Qualification Engineer I↗ Stemcell TechnologiesBurnaby, BC, CA $95k–$95k12d Lead commissioning, qualification, and validation activities for facilities, utilities, and laboratory equipment to ensure compliant and reliable operations.
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Clinical IT Quality Control Analyst - Remote US↗ McKessonRemote 12d Oversees quality control and assurance of software, process, and data integrity validation processes to ensure compliance with GxP and regulatory requirements.
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Senior Computer System Validation (CSV) Engineer↗ Xot Solutions Pte. Ltd.Singapore, S00, SG 12d Lead end-to-end validation and qualification of automated computer systems (IT/OT, MES, DCS, PLC, SCADA) in pharmaceutical manufacturing to ensure regulatory compliance.
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QA Professional DanaherBangalore, Karnataka, India 12d Support development, lifecycle management, and validation of digital tools, computerized systems, and AI-enabled applications for Regulatory Affairs and Quality Assurance operations.
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Spécialiste des systèmes de qualité/Quality Systems Specialist FreseniusmedicalcareVaudreuil-Dorion, QC, CAN 12d Ensures quality initiatives and compliance objectives for facility methods, procedures, validations, and quality planning across existing and new product designs.
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Validation Specialist 3 PciservicesMississauga, CAN, CA $75k–$75k12d Own high-risk validation projects for biopharma clients, ensuring compliance with cGMP/GAMP/21CFR standards and delivering validated processes for product/system launches.
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6518 - Service Order CQV Engineer / Validation Engineer↗ VeristaIndianapolis, IN, US 13d Provide technical CQV (commissioning, qualification, and verification) expertise on large capital projects involving new or modified equipment, facilities, and utilities in the life sciences industry.
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Validation Engineer FreseniusglobalGrand Island, NY $61k–$61k14d Validates and revalidates pharmaceutical products, equipment, and systems to ensure compliance with cGMPs and industry standards.
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Senior Specialist, Validation Engineer II BristolmyerssquibbDevens - MA - US $93k–$93k14d 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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Consultant - Business Consulting Risk - TMT - CNS - RISK - DIGITAL RISK - Mumbai↗ EYMH, IN 14d Consultant specializing in Computer System Validation (CSV) for Life Sciences clients to ensure compliance with regulatory requirements and internal procedures.
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CQV Engineer↗ Amaris Act Pte. Ltd.Tanjong Pagar, S00, SG 14d Support commissioning, qualification, and validation activities for pharmaceutical equipment and systems in a GMP environment.
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Prozessingenieur Validierung & Qualifizierung (m/w/d) Arbeitsort: Lorsch↗ Prisman GMBHMannheim, BW, DE 15d Develop and execute validation and qualification strategies for medical devices and hygiene products throughout the product lifecycle.
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Qualification and Validation Specialist↗ SanofiToluca, MEX, MX 15d Guardian of laboratory technical integrity, leading qualification and validation of equipment and instruments to ensure data traceability and regulatory compliance.
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Intern - IT Quality and Compliance LabcorpMadison WI 15d Support IT Quality and Compliance activities, specifically Computer System Validation (CSV) and periodic reviews for Drug Development Labs.
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Validation Engineer↗ Coalesce Management ConsultingSingapore, S00, SG 15d Develop and execute qualification documentation and testing for laboratory equipment to ensure compliance and readiness for routine operation in GMP-regulated environments.
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Validation Engineer Sterilization (MS&T) GaldermaUppsala 15d 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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