Computer System Validation
299 open positions
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Validation Engineer FreseniusglobalMelrose Park, IL $65k–$65k28d 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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Process Validation Engineering Co-Op DanaherFargo, North Dakota, United States $0k–$0k28d Support process validation activities across the biologics manufacturing lifecycle, including process design, qualification, and continued verification.
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Technical Services Supervisor (Cikarang Site) AstraZenecaIndonesia - Cikarang 28d Lead digital initiatives and support validation/qualification for IT systems in a pharmaceutical manufacturing environment.
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Senior Validation Engineer - CSV (OT) LonzaUS - Vacaville, CA $93k–$93k28d Leading and executing validation activities for manufacturing processes, equipment, computerized systems, and automation control systems to ensure compliance with regulatory requirements and internal quality standards.
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SAP Compliance Manager m/f/d↗ CordenpharmaLisboa, P11, PT 29d Ensure compliance, validation, and audit readiness for SAP S/4HANA and connected applications in a highly regulated pharmaceutical environment.
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CQV Engineer↗ Coalesce Management ConsultingSingapore, S00, SG 29d Plan, execute, and document commissioning and qualification (CQV) for pharmaceutical process equipment and temperature-controlled units in a GMP environment.
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Lab Validation↗ Anter Consulting Pte. Ltd.Singapore, S00, SG 29d Qualify and validate environmental monitoring equipment (air samplers, particle counters) in GMP-regulated pharma/biotech settings.
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MSAT Staff Scientist – Process Validation & Technology Transfer↗ Thermo Fisher ScientificPlainville, MA, US $103k–$103k29d Own process validation strategy and lifecycle execution for biologics and viral vector programs, serving as technology transfer lead for incoming client and internal programs.
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CSV/CQV Engineer – Kneat↗ Jc AutomationRemote 29d Develop, execute, and approve commissioning, qualification, and computer system validation (CSV/CQV) documentation for equipment, utilities, facilities, and automated systems in a regulated pharmaceutical manufacturing environment.
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Sr. Principal Quality Engineer CardinalhealthTN-LaVergne Pack, US $105k–$105k29d Develop and execute standardized cleaning validation protocols and master plans for a contract pharmaceutical packaging facility to ensure regulatory compliance.
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Senior QA Engineer COALESCE MANAGEMENT CONSULTING PTE. LIMITEDSingapore 1mo Provide independent quality oversight for Commissioning, Qualification, and Validation (CQV) activities for facilities, utilities, equipment, and systems in a GMP-regulated environment.
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Senior Computer System Validation (CSV) Engineer CaiMelbourne, Victoria 1mo Lead validation activities for GxP-regulated systems in an advanced therapeutics facility, ensuring compliance with regulatory frameworks and supporting data integrity programs.
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Packaging Engineer LivaNovaMelbourne, Victoria 1mo Ensure medical device packaging activities comply with GMP, ISO 13485/11607, and regulatory standards through validation, testing, and documentation.
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Sr. QA Computer System Validation Mgr. 4dmoleculartherapeuticsHybrid $126k–$126k1mo 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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Technical Process Engineer AbbottIreland - Donegal Town 1mo Support Technical Services (STARS lab) engineering, validation, and maintenance activities for FreeStyle blood glucose test strips and sensors.
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Computer Systems Engineer I CatalentKansas City, MO 1mo Maintain computerized laboratory, manufacturing, and production systems while ensuring regulatory compliance and data integrity in a GMP environment.
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Transformation Project Qualification Lead- API AbbVieNorth Chicago, IL, us 1mo Lead project teams to drive schedule, execution, risk management, and reporting for commissioning, qualification, and validation of new/modified equipment, facilities, utilities, and processes in line with project and quality objectives.
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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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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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Computerized Systems Validation (CSV) & Data Integrity Lead GehcCork 1mo Lead Computerized Systems Validation (CSV) and Data Integrity programs to ensure GxP system compliance, inspection readiness, and alignment with regulatory requirements.
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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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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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Senior Engineer Validation StrykerGurugram, India 1mo Execute validation activities (IQ/OQ/PQ) to industrialize and transfer new medical device products into manufacturing, ensuring compliance with regulatory standards.
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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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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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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 Software Testing Manager↗ MedpaceCincinnati, OH 1mo Manage a team of software testing engineers and validation projects to implement high-quality software solutions for regulated Medpace applications.
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IT Quality & Validation Specialist↗ Hikma PharmaceuticalsSintra, Lisbon, Portugal 1mo Execute Computer System Validation (CSV) for GxP systems, ensuring compliance with regulations like 21 CFR Part 11 and Annex 11 for Hikma's injectable pharmaceutical production.
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CSV Manager↗ ViatrisCounty Galway, Ireland 1mo Manage end-to-end Computerized System Validation (CSV) for GxP computerized systems to ensure regulatory compliance and maintain validated states.
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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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CSV Engineer / Senior CSV Engineer Singapore Advanced Manufacturing Tech Solutions PTE. LTD.Remote 1mo Execute Computerized System Validation (CSV) lifecycle activities, equipment qualification (IQ/OQ/PQ), and compliance reporting for GMP-regulated pharmaceutical systems.
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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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