Job Description Summary The QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs. Job Description Major accountabilities: Perform the analysis of batches following specific training; Promptly report to the Quality Control Supervisor and the Qualified Person any deviation and/or out of specification detected during the analysis activities. Collaborate with the Quality Control Head/supervisor for the CAPA implementation in the quality control department. Control processes, equipment and area. Perform routine maintenance and cleaning, periodic microbiological verification of pharmaceutical areas quality control equipment and support external specialized personnel in carrying out extraordinary maintenance/qualification activities. Perform incoming and outgoing verification activities of raw materials and materials. Collaborate with the Quality Control Head to the management of material stocks and waste materials. Collaborate with the Quality Control Head to the training of new personnel. Execute the calibration, verification, qualification and validation activities of the Quality Control processes and equipment. Essential requirements: Degree in CTF, Pharmacy, Chemistry. Previous experience in a similar role within a GMP environment. Available to work in shifts, including night shifts. Fluent in Italian. Good knowledge of English. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. J-18808-Ljbffr