Computer System Validation
302 open positions
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Team Member Qualifications Dr-Reddy-S-Laboratories-LimitedVisakhapatnam, in 1d Execute equipment and system qualification protocols (IQ, OQ, PQ) and support regulatory readiness in pharmaceutical manufacturing.
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Global Validation/Verification coordinator EurofinsBengaluru, KA, in 1d Coordinates global validation and verification of laboratory tests to ensure compliance with regulatory requirements and quality standards, overseeing documentation and QA reviews for successful test implementation.
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Business Analyst, Serialization & Traceability L3 Expert GaldermaKrakow, PL 1d Lead validation activities for serialization and traceability systems within the pharmaceutical IT landscape to ensure GxP compliance.
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Test Equipment and Method Validation Engineer ConvaTecReynosa, Mexico 1d Validation and qualification of processes and equipment, including establishing and maintaining Validation Master Plans (VMP) and local procedures in compliance with GHTF guidelines.
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Pharmaceutical Engineer - CQV (Contract - Tuas)↗ Rma Contracts Pte LtdSingapore, S00, SG 1d Lead Commissioning, Qualification, and Validation (CQV) activities for pharmaceutical manufacturing systems, ensuring compliance with C&Q Execution Plans and regulatory standards.
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Senior System Specialist PfizerUnited States - Massachusetts - Andover $99k–$99k1d Provide technical support, project management, and lifecycle management for cGMP instruments and workstations in Quality Control and Manufacturing environments.
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Industrial Automation and CSV Engineer - San Diego↗ Vti Life SciencesSan Diego, CA, US $80k–$80k1d Ensuring computerized systems in regulated environments are validated in compliance with industry standards and regulatory requirements while supporting PLC and SCADA controlled manufacturing systems.
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Process Validation Engineer RocheOceanside, US $81k–$81k1d Execute process validation protocols and regulatory documentation for drug substance manufacturing to ensure cGMP compliance and support product lifecycle activities.
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Validation Engineer (MNC/pharmaceutical)↗ Rrecruiter Int Pte. Ltd.Singapore, S00, SG 1d Execute CQV activities for GMP-regulated pharmaceutical and biopharmaceutical facilities, ensuring compliance with regulatory standards.
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Pharmaceutical Engineer - CQV (Contract - Tuas)↗ Rma ProjectsGeylang, S00, SG 1d Lead Commissioning, Qualification, and Validation (CQV) activities for pharmaceutical process areas, ensuring compliance with C&Q Execution Plans and regulatory standards.
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Computer System Validation (DeltaV)↗ Coalesce Management ConsultingOutram, S00, SG 1d Ensure validation and lifecycle management of automated and computerized systems within regulated manufacturing environments.
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Internship IBEX MSAT Validation 80-100% (m/w/d) LonzaSchweiz 2d Support process validation activities for Upstream and Downstream manufacturing operations in a biopharmaceutical setting.
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Senior/ QA Validation Executive (1- Year Contract) GlaxoSmithKline Pte LtdSingapore 2d Lead QA validation activities for new product introductions and transfers, ensuring compliance with quality systems and patient safety.
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Qualification Engineer | Pharma | Geel Select ProjectsGeel, Turnhout $32k–$32k3d Support the engineering team in qualifying equipment throughout its entire lifecycle at a leading pharmaceutical company.
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GxP Validation / Release Readiness SME Next-LinkBasel, Basel-Stadt 3d Senior specialist providing independent advisory support for validation, testing, deployment, cutover, go-live, and hypercare activities during pharmaceutical regulatory transformations.
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Technician, Validation III (temporary 6 months) AbbVieHeredia, Heredia Province, cr 3d Execute validation activities for processes, equipment, and computerized systems to ensure compliance with medical industry standards.
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QA Validation Specialist 3 ManpowerGroup NetherlandsMaastricht, Limburg $54k–$54k4d Reviewing, approving, and overseeing validation and qualification activities for equipment, facilities, utilities, and processes in a GMP-regulated pharmaceutical environment.
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Senior Specialist, Digital and Data Quality MsdUSA - North Carolina - Durham (Old Oxford) 4d Ensures quality and compliance of GMP computerized systems and supporting infrastructure across manufacturing, packaging, labeling, and laboratories to protect product quality and patient safety.
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Senior Validation Engineer↗ Interactive ResourcesGainesville, FL, US $125k–$125k4d Develops and executes validation protocols, supports risk-based validation strategies, and maintains compliance with quality systems and regulatory requirements for medical devices.
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Engineer II, QA↗ Thermo Fisher ScientificLogan, UT, US 4d Quality Engineer supporting bioprocessing equipment automation, manufacturing, and quality systems to ensure compliance with cGMP, ISO, and FDA standards.
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Quality Assurance Specialist PSC BiotechBrisbane, Queensland 4d Provide Quality Assurance oversight and support for commissioning, qualification, validation, technology transfer, and process lifecycle management in regulated industries.
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Qualité projet / Validation SI/Cloud F/H CTS CorporateAlbi, Tarn 5d Strategic and operational partner ensuring compliance of IT/Cloud deliverables and AI projects with strict pharmaceutical regulations (GAMP 5, FDA, EMA, EU Annex 11).
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Sterilization Validation Scientist (Fraser, MI)↗ GetingeFraser, MI, US $99k–$99k5d Design, validate, and sustain sterilization programs for medical devices, ensuring compliance with global regulatory standards for sterile barrier integrity and microbial performance.
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Sr. Mechanical Engineer↗ CognizantCiudad Juárez, CHH, MX 5d Mechanical Product Validation Engineer specializing in cleaning, sterilization, and reprocessing validation of reusable medical devices.
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Validation Analyst I CatalentKansas City, MO, US 5d Support validation and qualification programs across manufacturing and laboratory disciplines to ensure compliance with guidelines and regulatory requirements.
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NPSS Quality Assurance Manager PhilipsBangalore, IN 5d Lead and execute compliant, risk-based assurance for computerized systems supporting medical device quality and business processes.
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SW Tool Validation Lead Neko-HealthStockholm 5d Lead end-to-end software tool validation and computer system validation (CSV) for medical device systems, ensuring they are fit for intended use through a risk-based assurance approach.
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Consultant - Business Consulting Risk - TMT - CNS - RISK - DIGITAL RISK - Mumbai↗ EYMH, IN 5d Consultant specializing in Computer System Validation (CSV) for Life Sciences clients to ensure compliance with regulatory requirements and internal procedures.
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Senior/ QA Validation Executive (1- Year Contract) GskSingapore - Tuas 5d Lead QA validation activities for new product introductions and transfers, ensuring compliance with quality systems and patient safety.
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Validation Analyst 2 PciservicesRockford, IL, USA $0k–$0k5d Manage validation projects for intermediate customer accounts, ensuring compliance with government and customer requirements for biopharma processes and systems.
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Engineer CQV_BLS↗ ExentecDallas, TX, US 5d Execute and document system-level commissioning activities for BLS/Pharmaceutical projects, ensuring facilities, utilities, and equipment are safely completed, tested, and prepared for turnover.
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BIOPHARMACEUTICAL – C&Q Manager↗ MMR ConsultingTijuana, BCN, MX 5d Lead commissioning, qualification, and start-up of upstream/downstream bioprocess systems and facilities for biopharmaceutical clients.
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Qualification & Validation Engineer MedmixDnešice, Plzeň Region, cz 6d Designing, coordinating, and executing validation processes for new products and technologies in the medical device industry.
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Manager, Quality Engineering BaxterRound Lake, Illinois, US $112k–$112k6d Leads independent oversight of site validation programs and governance of plant data integrity to ensure compliance with cGMP and regulatory standards.
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Computerized Systems Validation Specialist SharpservicesHeerenveen, NL $46k–$46k6d Ensuring all IT systems impacting Good Manufacturing Practices are in a validated state and maintaining compliance with international regulations.
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CQV Engineer / Pharma / West / SGD 6,300!↗ Integrity PartnersOutram, S00, SG $6k–$6k6d Plan, execute, and document CQV activities (IQ, OQ, PQ) for pharmaceutical manufacturing facilities, utilities, and process equipment.
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Senior Manager, Global R&D Audits & Inspections Readiness↗ Beone MedicinesRemote, US 6d Execute validation-by-design, audit readiness, and compliance execution for R&D technology solutions to ensure continuous regulatory compliance and inspection readiness.
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Validation Technician SoterahealthRantigny, FR 6d Support the validation coordinator in managing client validations, thermal mapping, and inventory for sterilization and lab testing processes.
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