Computer System Validation
333 open positions
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Senior Specialist, Associate Aseptic Process Validation Engineer BristolmyerssquibbDevens - MA - US $88k–$88k2mo Supports the execution of Aseptic Process Simulations/Validations (APS/APV) and Aseptic Performance Qualifications for the Devens Cell Therapy Facility.
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QC Validation Lead GsknchMalaysia - Kuala Lumpur 2mo Lead and coordinate all validation activities within the Quality Control department to ensure laboratory operations, analytical methods, equipment, and computerized systems perform as intended and remain compliant with regulatory requirements.
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Quality Engineer II JabilBettlach, CH 2mo Lead validation strategies and quality initiatives for new product introductions, technology implementations, and manufacturing changes to ensure compliance and product quality in regulated industries.
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Senior QA Specialist RegeneronLimerick $54k–$54k2mo Leading and supporting Quality Assurance activities for technology transfer projects, ensuring effective knowledge transfer, risk management, and implementation of quality requirements for new manufacturing technologies and digital solutions.
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CSV Engineer – DeltaV (pharmaceutical)↗ Kingsforce Management Services Pte. Ltd.Bukit Merah, S00, SG 2mo Plan, execute, and manage DeltaV Computer System Validation (CSV) lifecycle activities for pharmaceutical manufacturing systems.
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CQV Engineer - Analytical/QC Laboratory Equipment↗ Anter Consulting Pte. Ltd.Singapore, S00, SG 2mo Commissioning, qualification, and validation of analytical and QC laboratory equipment to ensure GMP and regulatory compliance.
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HVAC Commissioning Engineer↗ Process Engineering Specialists Pte. Ltd.Singapore, S00, SG 2mo Perform commissioning and qualification (IQ/OQ/PQ) of GMP HVAC systems and cleanroom facilities for Life Sciences clients.
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Validation Engineer II BarrywehmillerIndianapolis, IN 2mo Develop and execute validation and FDA compliance documents/protocols for pharmaceutical equipment and processes, including process equipment, facility/utilities, and cleaning systems.
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Validation Engineer II EmpowerpharmacyHouston, TX 2mo Drives compliance and manufacturing readiness across sterile and non-sterile operations through equipment, process, and computer system validation.
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Qualification & CSV Specialist | Freelancer SgsLisboa, Lisboa, pt 2mo Execute equipment, facility, and system qualification and computerized system validation (CSV) activities for pharmaceutical, biotech, and medical device projects.
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MES Change Specialist RocheHillsboro, US $79k–$79k2mo Design, build, test, validate, and maintain electronic documentation and Manufacturing Execution Systems (MES) for pharmaceutical production and packaging.
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QA Specialist↗ CaiSydney, New South Wales, Australia 2mo Ensuring operational readiness and compliance for FDA-regulated industries through commissioning, qualification, and validation services.
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Tecnico di Convalida – Calibratore Pharma Veolia Environnement SAVerona, Veneto, it $25k–$32k2mo Execute technical qualification, validation, and calibration of instruments and equipment within pharmaceutical production processes.
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Automation Engineer - Engineer / Senior Engineer - Programming (Managed by Klenzaids Contamination Controls Pvt. Ltd.) SyntegonGoa, GOA, in 2mo Developing and maintaining automation software and tools for cleanroom, bio-safety, and sterilization systems used in pharmaceutical and biotech manufacturing.
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?R&D Engineer – Qualification & Validation (m/w/d) - befristet auf 3 Jahre Hechingen, BADEN_WUERTTEMBERG 2mo Ensure compliance and quality of dialysis devices, methods, and systems through qualification and validation activities in a regulated MedTech environment.
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Principal Automation Engineer AgilentUS-CO-Frederick $147k–$147k2mo Lead automation projects for large-scale greenfield pharmaceutical manufacturing facility design, construction, and operation.
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Computer Systems Validation Engineer LonzaUS - Portsmouth, NH 2mo Identify and implement industry best practices for computer systems validation (CSV) in biotech/pharma manufacturing, ensuring compliance with regulations like 21 CFR Part 11 and GAMP.
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Validation Engineer | Equipment & Process Qualification – Vilnius ThermofisherVilnius, Lithuania $26k–$26k2mo Ensure equipment, systems, facilities, and processes are properly qualified, compliant, and ready for reliable operations in manufacturing and laboratory environments.
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CHARGE(E) DE VALIDATION DES SYSTEMES INFORMATIQUES- CDI H/F EurofinsLes Ulis, IDF, fr $34k–$38k2mo Implementing and validating computerized systems and developing PowerApps for pharmaceutical quality control sites.
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Validation Engineer II MedlineShanghai 上海, CN 2mo Provide technical support for sterile packaging projects to ensure regulatory compliance and maintain quality standards across Medline product divisions.
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Mes Scrum Master (English & Italian Speaking) Tachyon Technologies LLCItalia $31k–$31k3mo Facilitate Agile software development and validation processes for pharmaceutical MES systems, ensuring compliance with GxP regulations.
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Chargé AQ Validation des systèmes informatisés / Data Integrity Officer - F/H (CDI) PolyPeptide FranceStrasbourg, FR 3mo Ensure compliance with regulations (GMP, 21CFR Part 11, Annex 11) and group/local procedures for computerized system validation and data integrity at the Strasbourg site.
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Validation & Qualification Manager Bi Ah ItNoventa Padovana, Provincia di Padova 3mo Leading validation and qualification activities for sterile veterinary vaccine manufacturing, ensuring GMP compliance for biological and immunological products.
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Manager, QA Method Validation NovartisCarlsbad $114k–$114k3mo Leading laboratory method validation for assays and devices in clinical and GMP settings to ensure compliance and data quality for breakthrough therapies.
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Senior Computer Systems Validation Engineer VaxcyteSan Carlos, California $164k–$164k3mo Leading validation activities for cloud-based GxP systems to ensure regulatory, quality, and operational compliance throughout the system lifecycle.
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Sr. Validation Engineer II TakedaUSA - CA - Thousand Oaks - Rancho Conejo $116k–$116k3mo Lead execution of equipment, systems, facilities, and utilities qualification (CD, DQ, IQ, OQ, PQ, CV) in a regulated pharmaceutical manufacturing environment.
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Test Engineer, Functional ValgenesisLisbon 3mo Functional testing of enterprise software within the life sciences product development lifecycle to ensure compliance and manufacturing excellence.
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Ingénieur qualité/Ingénieure qualité CleevenBraud-et-Saint-Louis, L'Estuaire 3mo QA Engineer specializing in process and cleaning validation to ensure regulatory compliance of pharmaceutical operations.
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QA Digital Compliance Manager AbbVieCampoverde, Lazio, it 3mo Ensuring digital systems, records, and data handling in pharmaceutical operations adhere to regulatory standards like FDA 21 CFR Part 11 and EU Annex 11.
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QA Officer Validation SharpservicesHamont-Achel, BE 3mo Ensuring validation of systems, processes, installations, and equipment within a pharmaceutical organization to meet regulatory standards and client requirements.
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Computer Systems VALIDATION ENGINEER↗ European Tech RecruitDublin, County Dublin, Ireland 3mo Lead computer systems validation (CSV) activities for automation and digitalization projects in pharmaceutical manufacturing.
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Computer System Validation (CSV) Engineer↗ Kashiv Biosciences LLC.Piscataway, NJ, US 3mo Plan, author, and execute validation deliverables for regulated systems including laboratory instrumentation, engineering/manufacturing equipment, and enterprise platforms to ensure compliance with 21 CFR Part 11, GxP, and EMA requirements.
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MSAT Engineer – Cleaning Validation TG SingaporeSingapore 4mo Support GMP-regulated pharmaceutical and biopharmaceutical manufacturing operations by managing cleaning validation lifecycle activities, executing validation strategies, and ensuring compliance with regulatory standards.
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Associate Manager - MSAT (C&Q) PfizerIndia - Vizag 4mo Evaluate, review, and approve validation master plans, protocols, and reports for sterile dosage form facilities to ensure compliance with regulatory requirements and company standards.
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Validation Specialist IS (GxP) -CDI- F/M PierrefabreHaute Garonne (31) 4mo Ensure GxP Information Systems (on-premise and cloud) are validated, compliant, and maintained in a validated state throughout their lifecycle for R&D Pharma systems.
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Chargé(e) de validation - h/f SimagecFuveau, Trets 4mo Conducting process validations for medical device packaging and aseptic pharmaceutical distribution in cleanroom environments, ensuring compliance with regulatory standards.
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Validation QA Engineer WuXi AppTecSingapore 4mo Managing validation activities for equipment, facilities, cleaning, water systems, and utility gases to ensure GMP compliance and production safety.
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Quality Engineer Coalesce Management ConsultingSingapore 4mo Supporting and reviewing MES validation activities, ensuring data integrity, and maintaining documentation compliance for manufacturing processes.
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