Computer System Validation
589 open positions
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IT Sofware Validation Engineer↗ FlexAguascalientes, AGU, MX 15d Develops and executes Computer System Validation (CSV) activities for software applications supporting medical device manufacturing and quality systems.
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Pharma Validation Facility Engineer↗ Katalyst Healthcares & Life SciencesCincinnati, OH, US 15d Leading maintenance, engineering, and validation activities for clinical packaging equipment, facilities, utilities, and cleaning processes to ensure regulatory compliance and product quality.
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Validation Engineer | Bentley Labs↗ ThgEdison, NJ, US $95k–$110k15d Develop and execute validation protocols (IQ, OQ, PQ) for compounding, blending, and packaging equipment in a cGMP manufacturing environment.
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Ingeniero de validación↗ Phillips MedisizeQuerétaro, Querétaro, Mexico 15d Realizar actividades de validación en etapas previas a producción para asegurar que productos y procesos médicos cumplan con los requisitos del cliente.
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QA Validaciones↗ Randstad España 15d Lead and ensure all company systems comply with quality standards and international regulations, guaranteeing data integrity in a continuous improvement environment.
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Projektledare, valideringsledare och valideringsingenjörer inom Life Science i Stockholm och Uppsala↗ JobbsafariStockholm, Stockholm County, Sweden 15d Lead and execute validation projects for equipment, processes, and computerized systems in Life Science manufacturing environments, ensuring compliance with regulatory requirements.
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Técnico/a Cualificaciones↗ Ultimate SolutionsAlcobendas, Community of Madrid, Spain 15d Develop documented evidence to ensure pharmaceutical client teams, processes, and systems comply with regulatory requirements and specifications for intended use.
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Ingeniero de validación↗ HaysMadrid, Community of Madrid, Spain 15d Lead engineering, facility improvements, and production equipment validation projects to ensure GMP compliance and quality standards.
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Valideringsledare inom Produktion, Life Science↗ Knightec GroupSolna, Stockholm County, Sweden 15d Lead and drive validation work for Life Science projects, ensuring processes, systems, and equipment meet regulatory requirements and standards.
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Validation Engineer I (Medical Indsutry)↗ Bepc Inc. - Business Excellence Professional ConsultingGuadalupe, Nuevo León, Mexico 15d Provide technical engineering support for validation activities, ensuring compliance with GMP and GDP in manufacturing and medical device environments.
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Validation Engineer - Experienced BarrywehmillerRaleigh, NC, US 15d Develop and execute validation protocols and FDA compliance documents for pharmaceutical equipment and automated systems.
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Senior Executive-QA Piramal PharmaIndia 15d Ensuring quality compliance and validation of equipment, facilities, and processes in a pharmaceutical CDMO environment.
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Senior Specialist - Quality Assurance (Validation) Pharmagend Global Medical Services Pte. Ltd.Singapore 16d Lead qualification and validation activities for equipment, utilities, facilities, processes, and computer systems in a pharmaceutical manufacturing environment to ensure regulatory compliance.
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Vi söker underleverantörer och erfarna specialister inom Life Science↗ Randstad SwedenUppsala, Uppsala County, Sweden 16d Specialist contractor role for validation and process engineering in the Life Science sector, serving pharmaceutical and medtech clients in the Uppsala region.
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QA-Documentation Engineer↗ Esteril Process SolutionsMumbai, Maharashtra, India 16d Develop and maintain technical quality and validation documentation (FDS, DQ, IQ, OQ, FAT) for process equipment and systems.
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Chargé d'Etudes Validation de Process F/H B.BRAUN MEDICALNogent-le-Rotrou, Eure-et-Loir 17d Ensure qualified and validated state of production equipment and processes in a medical device manufacturing facility, ensuring compliance with regulations and standards.
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Consultant validation systèmes informatisés en life sciences F/H PharmasysLyon, Rhône 17d Lead digital transformation and validation of computerized systems for Life Sciences clients, ensuring compliance with regulations and quality standards.
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COMPUTER SYSTEM VALIDATION & DATA INTEGRITY CONSULTANT - AMBITO GCP OrientaProvincia di Verona, Veneto €30k–€40k17d Managing Computer System Validation (CSV) activities and Data Integrity requirements for GCP-compliant systems in the regulatory consulting sector.
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CQV / COMMISSIONING ENGINEER↗ Regional EnergySingapore, S00, SG 17d Commissioning and qualification of process equipment, packaged equipment, and process skids for a pharmaceutical manufacturing facility.
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Senior C&Q Engineer - Device Assembly and Packaging↗ Biopharma Consulting Jad GroupJuncos, PR, US 17d Lead commissioning and qualification for device assembly and packaging equipment, managing the full validation lifecycle from strategy to characterization reports.
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?Engineer↗ Humacao, PR, US 18d Support Test Method Validation (TMV) activities, Change Control processes, and technical documentation within regulated industries.
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Senior Project Engineer Commissioning & Qualification JjGeel, Antwerp, Belgium €73k–€115k18d End-to-end ownership of qualification strategy for Atlas process equipment at a commercial API plant, ensuring safe and compliant delivery of medicines.
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Test Engineer StrykerBelfast, United Kingdom £33k–£56k18d Provide design, technical, and operational support to test processes and manufacturing validation for Pad-Pak capacity expansion in a medical device environment.
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Principal Validation Engineer, CVRM RocheHolly Springs, US $95k–$176k18d Develops, implements, and maintains validation status of application equipment and manufacturing processes for high-volume drug product manufacturing.
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2027 Validation Engineer Co-Op (July - Dec) (Undergraduate) AbbVieWorcester, MA, us 19d Support the planning and execution of validation tasks for manufacturing and Quality Control systems, ensuring compliance with cGMP practices and Global Quality Systems.
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Quality Assurance Manager* (m/w/d) Qualifizierung/Validierung Lgc-GroupBerlin, BE, de 19d Manage GMP-compliant Quality Management System (QMS), develop processes and standards, and oversee qualification and validation activities for facilities, equipment, utilities, and computerized systems in a life science/pharmaceutical context.
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Application V&V Engineer (m/f/d) DanaherSchweiz 19d Lead verification and validation (V&V) of applications interfacing with multiple subsystems in life sciences and diagnostics, ensuring compliance with regulatory standards and quality management systems.
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Facilities Engineer↗ Eqval Consulting Group, Inc.Ponce, PR, US 19d Develop, review, and execute qualification and validation protocols for Compressed Air Systems, Dryers, and Air Handling Units in a clean medical device manufacturing facility.
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QC/QA Engineer (Biotech)↗ PersolOutram, S00, SG 19d Subject matter expert for assigned equipment or systems performance to ensure safety, compliance and sustained operation.
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?Senior Specialist - Quality Assurance (Validation)↗ Jurong Island, S00, SG 19d Preparation and execution of qualification and validation activities for equipment, utilities, facilities, processes, and computer systems in compliance with regulatory guidelines.
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CQV Manager↗ Legend BiotechRaritan, NJ, US 19d Leading and overseeing Commissioning, Qualification, and Validation (CQV & CSV) activities for a cGMP clinical and commercial cell therapy manufacturing facility to ensure systems remain compliant and fit for intended use.
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QA Validation Professional – P2↗ CepheidKA, IN 19d Supporting quality systems activities related to software validation, focusing on design control and risk management in accordance with FDA and ISO regulations.
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Senior Pharmaceutical Project Manager JciIndianapolis-Indiana-United States of America 19d Senior project leader for validated environment and laboratory construction programs (cleanrooms, biosafety cabinets, containment suites) across campus or multi-site portfolios.
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QA Specialist II (Validations) PciservicesLeon, Spain 19d Ensure compliance with GMP standards and regulations across pharmaceutical operations, covering equipment, systems, processes, and documentation to guarantee product quality and safety.
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Senior CQV Engineer (m/w/d) Life Sciences AfryMannheim, BW, de 20d Central point of contact for Commissioning, Qualification & Validation (CQV) within Life-Science projects, ensuring pharmaceutical and biotechnological systems are GMP-compliant, tested, documented, and handed over to operators.
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Testovací inžinier pre HMI a PLC (Alarm & Function Testing) (m/ž) SyntegonRemote 20d Testing, verifying, and documenting alarm and function performance of pharmaceutical production lines (PLC and HMI) according to GMP validation standards.
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Associate Manager, Engineering - Validation LonzaSingapore 20d Manage the validation lifecycle program for facility and equipment utilities to ensure compliance with regulatory requirements in pharmaceutical manufacturing.
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GCP - Computer System Validation Specialist (12 month limited-term) AlimentivLondon, Ontario 20d Validate GCP-regulated computerized systems and software to ensure compliance with 21 CFR Part 11 and quality system principles in a pharmaceutical/biotech environment.
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QC Qualification Engineer (Laboratory Analytical Computerised Systems)↗ Anter Consulting Pte. Ltd.Singapore, S00, SG 20d Own the qualification lifecycle of laboratory analytical computerised systems, including validation, change control, and decommissioning.
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ENGINEER QUALITY↗ Nice-Pak Products LLCSt. Louis, MO, US 20d Develop documentation and validate facility systems and processes to ensure compliance with FDA regulations and GMPs for food, drug, and cosmetic industries.
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CSV Validavimo Inžinierius (-ė) | Kompiuterizuotos ir automatizuotos sistemos ThermofisherVilnius, Lithuania €26k–€39k20d Engineer responsible for validating computerized and automated systems in manufacturing, laboratory, quality, and technical operations environments to ensure reliability and regulatory compliance.
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Quality Engineer - Medical Device - Contract↗ Vti Life SciencesPendleton, SC, US 20d Lead and coordinate validation execution activities for special processes (laser marking, welding) in medical device manufacturing.
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Audit Supervisor↗ Oxford Global ResourcesRemote 20d Coordinate evidence collection for GxP regulatory inspections and customer audits, analyze audit data, and improve audit support processes using data analytics.
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