Ph3Experteer Overview /h3pIn this role you will lead AST 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/AST, partnering across internal and external teams to deliver reliable, compliant testing and data-driven decisions. /ph3Retribuzione / Benefits /h3ulliLead and coordinate AST laboratory activities to align with production plans /liliDevelop, validate, transfer, maintain, and monitor analytical methods through their lifecycle /liliOversee method transfers to TRD, sites, and third parties; support investigations and CAPA implementation /liliEnsure GMP, GLP, QMS, pharmacopoeia standards, and regulatory dossier compliance /liliPlan and manage QC AST activities, including stability studies and risk management /liliEvaluate and qualify new technologies and laboratory equipment per regulatory and company standards /liliProvide technical support to QC, including investigations and continuous improvement projects /liliOversee documentation, SOP management, training, safety practices, and cross-functional collaboration /li /ulh3Responsabilità /h3ulliMaster degree in Pharmacy or Chemistry (or broad QC experience) /liliFluent in Italian; good knowledge of English /liliAt least 5 years of experience in a Quality Control department within the pharmaceutical industry /li /ul /p #J-18808-Ljbffr