Experteer OverviewIn Grünenthal's Manufacturing & Global Operations, you help safeguard product quality across the value chain by leading change controls, PQR issuance, CAPA-driven improvements, and master data validation. You collaborate with cross‐functional teams to ensure regulatory compliance and licensing obligations are met while driving continuous quality improvements. This role offers hands‐on QA responsibilities with meaningful impact on patient safety and product excellence.ResponsibilitiesManage change controls across sitesPlan and execute site trainingsIssue and revise Product Quality Reviews (PQR)Participate in self-inspections and CAPA managementRevise Master Batch RecordsIssue validation protocols and reportsParticipate in risk assessment managementCooperate in revising qualification and validation documentationOversee Quality Agreement with customersSupport regulatory activities to maintain manufacturing licensesCollect and monitor site KPIsQualificationsDegree in Scientific disciplines3–5 years of experience in Quality Assurance within pharmaceutical sectorKnowledge of local and international regulatory requirements and GMP standardsCompetency in communication and interfaces managementFluent EnglishBenefitsPerformance-based annual bonusEqual employment opportunities
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📌 Quality Assurance Officer (Italia)
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📍 Italia