Analytical QC & AS&T Expert

Experteer Overview

In 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 / Benefits

• Lead and coordinate AS&T laboratory activities to align with production plans
• Develop, validate, transfer, maintain, and monitor analytical methods through their lifecycle
• Oversee method transfers to TRD, sites, and third parties; support investigations and CAPA implementation
• Ensure GMP, GLP, QMS, pharmacopoeia standards, and regulatory dossier compliance
• Plan and manage QC & AS&T activities, including stability studies and risk management
• Evaluate and qualify new technologies and laboratory equipment per regulatory and company standards
• Provide technical support to QC, including investigations and continuous improvement projects
• Oversee documentation, SOP management, training, safety practices, and cross-functional collaboration

Responsabilità

• Master degree in Pharmacy or Chemistry (or broad QC experience)
• Fluent in Italian; good knowledge of English
• At least 5 years of experience in a Quality Control department within the pharmaceutical industry