Experteer OverviewIn this Site Quality Head role, you shape and safeguard the quality strategy for a complex Ivrea manufacturing site. You partner with site and global leadership to ensure compliant operations, continuity, and innovative improvements. You drive a strong quality culture while supporting launches and ensuring every product release meets safety and regulatory standards. You will lead a multidisciplinary quality organization and be pivotal in Health Authority engagements. This position offers high-visibility impact and strategic influence.Retribuzione / BenefitsLead the site Quality strategy to ensure full cGMP and regulatory compliance with corporate standardsEstablish and sustain a governance model and decision-making framework for the site quality organizationOwn and manage site quality systems including deviations, investigations, change control, PQ reviews, and documentation lifecycleEnsure inspection readiness and coordinate Health Authority inspections and follow-upsAct as Qualified Person (Deputy) overseeing batch certification and release per legal requirementsDrive quality risk management, escalation processes, and timely health authority notificationsCultivate a strong quality culture through training, self-inspections, and continuous improvement initiativesProvide leadership input for talent development, succession planning, and launch readinessLead and develop quality leaders and teams to sustain performance and regulatory excellenceResponsabilitàBachelor's degree in a scientific disciplineMinimum five years of experience in pharmaceutical Quality Assurance or Quality Control in a regulated manufacturing environmentStrong knowledge of cGMP and pharmaceutical quality management systemsProven experience leading quality organizations with people management and performance oversightDemonstrated experience preparing for, hosting, and responding to Health Authority inspectionsFluent English, written and spoken, in global cross-functional contexts
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