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Experteer OverviewAs a Junior CSV Specialist, you will help ensure computer systems used in life sciences stay validated and compliant. Si candidi qui sotto dopo aver letto tutti i dettagli e le informazioni di supporto relative a questa opportunità di lavoro. You will work with cross‐functional teams to apply GxP concepts and manage validation documents throughout the system lifecycle. This role offers international development opportunities and a clear path to grow within CSV and regulatory domains. You will gain hands‐on exposure to audits and real‐world validation challenges, contributing to high‐impact healthcare projects.Retribuzione / BenefitsDevelop validation strategies and manage lifecycle documentation (planning, requirements, design, testing protocols, release and maintenance) in line with GAMP5 and SOPsEnsure regulatory compliance (cGMP, GCP, Data Integrity) across validated systems and maintain lifecycle documentationEnforce CSV methodology within project teams and support GxP System Risk Assessment with stakeholdersOversee system change requests and related documentationCollaborate with technical teams to investigate validation incidents and implement solutionsReview proposed changes for validation implications to maintain validation statusSupport Senior CSV Specialist during client audits and regulatory inspectionsResponsabilitàRecent xrdztoy graduate with little or no experience in CSVFluent EnglishStrong interest in Life Science and PharmaKnowledge of computer information requirements legislation (privacy)Requisiti fondamentaliinternational opportunities for developmentflexible work policiescompetitive compensation packagesalary packagecorporate bonusmeal vouchers','Career development','Corporate training #J-18808-Ljbffr