Summary Work in the Sterile Area for aseptic manufacturing in accordance with the GMP requirements, Novartis SOPs and production documentation. About the Role Responsibilities include working in shifts to prepare and produce batches, performing routine maintenance and cleaning, conducting periodic microbiological verification of pharmaceutical areas and equipment, supporting external specialized personnel in extraordinary maintenance/qualification activities, promptly reporting deviations and out-of-specification events to the Production Manager and Qualified Person, performing incoming and outgoing verification of raw materials and materials, collaborating with the Production Manager to manage material stocks, waste materials, and train new personnel. Key Responsibilities Working in shifts, perform the necessary activities for the preparation and production of batches. Perform routine maintenance and cleaning, periodic microbiological verification of pharmaceutical areas and equipment and support external specialized personnel in carrying out extraordinary maintenance/qualification activities. Promptly report to the Production Manager and the Qualified Person any deviation and/or out of specification detected during the production process. Perform incoming and outgoing verification activities of raw materials and materials. Collaborate with the Production Manager to the management of material stocks and waste materials. Collaborate with the Production Manager to the training of new personnel. Essential Requirements Scientific/technical background. Willing to work in shifts, including night shifts and weekends. Fluent in Italian. Good knowledge of English. 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. Benefits and Rewards Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: #J-18808-Ljbffr