As Lead QA Technician, you ensure product quality and regulatory compliance within pharmaceutical manufacturing. You will work as part of the Quality team to uphold high standards and support life-changing medicines. Expect to investigate deviations, manage CAPA, and help prepare for regulatory inspections in an aseptic environment. You will collaborate with cross-functional teams to maintain compliant documentation and processes, contributing to the mission of making the world healthier, cleaner and safer. This role offers the chance to shape quality programs in a global, fast-paced setting.La preghiamo di verificare di possedere il livello di esperienza e le qualifiche adeguate leggendo la panoramica completa di questa possibilità qui sotto.Quality oversight of pharmaceutical manufacturing operationsBatch record review and deviation investigationsCAPA management and effectiveness verificationSupport regulatory inspections and customer auditsMaintain and improve quality systems and documentation (TrackWise,



Documentum)Collaborate with cross-functional teams to address quality issuesEnsure aseptic manufacturing processes and clean room controlsCommunicate findings clearly and drive corrective actionsGuide and develop team members on quality practicesManage multiple priorities in a dynamic environment4 years of experience in pharmaceutical quality assurance or related GMP environmentComprehensive knowledge of GMP regulations, FDA guidelines and quality systemsExperience with batch record review, deviation investigations and CAPA managementStrong understanding of aseptic manufacturing processes and controlsAdvanced proficiency in quality documentation systems (e.G. TrackWise, Documentum)Professional communication skills (written and spoken)Ability to manage multiple priorities and work under pressureStrong attention to detail and analytical problem-solving skillsInterpersonal and xysqume communication abilities; project management and organizational capabilitiesExperience supporting regulatory inspections and customer auditsCross-functional team collaborationProficiency with Microsoft Office applicationsKnowledge of root cause analysis and quality improvement toolsExperience with clean room operations and gowning procedures preferredAbility to interpret technical procedures and specificationsAs Lead QA Technician, you ensure product quality and regulatory compliance within pharmaceutical manufacturing. You will work as part of th…#J-18808-Ljbffr

📌 Audit Specialist (Monza)
🏢 Experteer Italy
📍 Monza