QO Expert
Pubblicato il 30-09-2026 - Zoetis in Catania
h3Rôle Description /h3 pEffettuare le attività di revisione e valutazione della documentazione di produzione dello stabilimento, assicurando il rispetto dei requisiti di conformità ed un adeguato tempo di rilascio dei lotti. /p h3DUTIES AND RESPONSIBILITIES /h3 ul liVerifica la completezza e la corretta compilazione, secondo i requisiti di Assicurazione qualità dei Batch Record Reports generati dal Reparto di Produzione e provvede alla loro approvazione preliminare; /li liAssicura che i controlli sui Batch Record Reports vengano eseguiti in conformità alle procedure vigenti e nelle tempistiche previste; /li liValuta le deviazioni aperte dai reparti e verifica lo stato di eventuali deviazioni, in corso presso i reparti di produzione di prodotti APIs e prodotti finiti prima dell'approvazione dei lotti; /li liAssicura attraverso ispezioni periodiche interne che vengano rispettate le GMP nelle aree di produzione prodotti API e magazzini. /li liEffettua insieme al QO Lead Audit interni nei reparti e si occupa della preparazione dei report. /li liSi occupa di stampare i documenti necessari alla produzione; Supporta il QO Lead nella gestione di batch note e deviazioni durante le attività di produzione. /li /ul h3Education /h3 ul liDiploma di Scuola Media Superiore; Laurea in Chimica, CTF, Scienze Biologiche /li /ul h3Experience /h3 ul liConoscenza dei principi che regolano la gestione aziendale della Qualità. /li liConoscenza dei processi di produzione, dei flussi di laboratorio e dei servizi al Manufacturing. /li liConoscenza approfondita delle Norme di Buona Fabbricazione, delle procedure del Sito e della Compagnia. /li liBuona conoscenza della lingua inglese. /li /ul h3CORE COMPETENCIES /h3 ul liBuona Conoscenza delle GMP. /li liBuona capacità comunicativa.
/li liCapacità di risolvere i problemi indipendentemente. /li liRispetto dei Zoetis Core Beliefs. /li /ul h3Role Description /h3 pPerform review and assessment activities of manufacturing documentation to ensure compliance with applicable quality requirements and timely batch disposition and release. /p h3KEY DUTIES AND RESPONSIBILITIES /h3 ul liReview Batch Record Reports generated by the Manufacturing Department for completeness, accuracy, and compliance with Quality Assurance requirements, and perform preliminary approval. /li liEnsure Batch Record Review reviews are conducted in accordance with approved procedures and within established timelines. /li liAssess deviations initiated by operational departments and verify the status of any ongoing deviations within API and Finished Product manufacturing areas prior to batch approval. /li liConduct periodic internal inspections to verify compliance with current Good Manufacturing Practices (cGMP) in API manufacturing areas and warehouse operations. /li liParticipate with the Quality Oversight (QO) Lead in conducting internal audits of manufacturing departments and support the preparation of audit reports. /li liPrint and issue manufacturing documentation required to support production activities. /li liSupport the QO Lead in the management of batch records, investigations,
and deviations during manufacturing operations. /li /ul h3QUALIFICATIONS EDUCATION /h3 ul liHigh School Diploma required. /li liBachelor's Degree in Chemistry, Pharmaceutical Chemistry and Technology (CTF), Biological Sciences, or a related scientific discipline preferred. /li /ul h3EXPERIENCE /h3 ul liKnowledge of Quality Management System (QMS) principles and quality governance processes. /li liUnderstanding of manufacturing processes, laboratory workflows, and manufacturing support services. /li liThorough knowledge of Good Manufacturing Practices (GMP), site procedures, and corporate quality standards. /li liGood command of written and spoken English. /li /ul h3CORE COMPETENCIES /h3 ul liStrong knowledge of GMP regulations and compliance requirements. /li liEffective communication and interpersonal skills. /li liAbility to independently identify, analyze, and resolve problems. /li liCommitment to and demonstration of Zoetis Core Beliefs and values. /li /ul h3About Zoetis /h3 pAt Zoetis, our purpose is to nurture the world and humankind by advancing care for animals. As a Fortune 500 company and the world leader in animal health, we discover, develop, manufacture and commercialize vaccines, medicines, diagnostics and other technologies for companion animals and livestock. We know our people drive our success. Our award-winning culture, built around our Core Beliefs, focuses on our colleagues' careers, connection and support. We offer competitive healthcare and retirement savings benefits, along with an array of benefits, policies and programs to support employee well‑being in every sense, from health and financial wellness to family and lifestyle resources. /p h3Global Job Applicant Privacy Notice /h3 #J-18808-Ljbffr