Experteer OverviewIn this role you will lead AS&T lab activities aligned with production needs, develop and validate analytical methods, and support QC and regulatory compliance to ensure quality medicines. You'll manage method transfers, investigations, and CAPA, while driving continuous improvement and the adoption of new technologies. The position sits at the heart of QC/AS&T, partnering across internal and external teams to deliver reliable, compliant testing and data-driven decisions.Retribuzione / BenefitsLead and coordinate AS&T laboratory activities to align with production plansDevelop, validate, transfer, maintain, and monitor analytical methods through their lifecycleOversee method transfers to TRD, sites, and third parties; support investigations and CAPA implementationEnsure GMP, GLP, QMS, pharmacopoeia standards, and regulatory dossier compliancePlan and manage QC & AS&T activities, including stability studies and risk managementEvaluate and qualify new technologies and laboratory equipment per regulatory and company standardsProvide technical support to QC, including investigations and continuous improvement projectsOversee documentation, SOP management, training, safety practices, and cross-functional collaborationResponsabilitàMaster degree in Pharmacy or Chemistry (or broad QC experience)Fluent in Italian; good knowledge of EnglishAt least 5 years of experience in a Quality Control department within the pharmaceutical industry
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