Ph3Summary /h3 pHighly skilled and experienced laboratory professional who contributes by performing analytical release testing, investigational support, research support, and stability testing. /p h3Major Accountabilities /h3 ul liLead and ensure execution of AST laboratory activities, aligning with plans, priorities, and production needs. /li liDevelop, validate, transfer, maintain, and monitor analytical methods throughout their lifecycle, in collaboration with TRD and external partners. /li liOversee analytical method transfers (TRD, sites, third parties) and support troubleshooting, investigations (OOS, deviations), and CAPA implementation. /li liEnsure compliance with GMP, GLP, QMS, pharmacopoeia standards, and regulatory dossier requirements. /li liPlan and coordinate QC AST analytical activities, including stability studies, method performance monitoring, and risk management initiatives. /li liEvaluate, implement, and qualify new technologies and laboratory equipment according to regulatory and company standards. /li liProvide technical and analytical support to QC, including investigations and continuous improvement projects for quality, safety, and efficiency. /li liEnsure proper documentation, SOP management, training, safety practices, stakeholder collaboration, and effective communication across internal and external teams. /li /ul h3Essential Requirements /h3 ul liMaster degree in pharmacy or chemistry, or broad experience in QC environment. /li liFluent in Italian. Good knowledge of English. /li liAt least 5 years in a Quality Control department within the pharmaceutical industry. /li /ul /p #J-18808-Ljbffr