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 background.
• Previous experience in a similar role within a GMP environment.
• Willing to work in shifts, including night shifts.
• Fluent in Italia. 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? http://www.novartis.com/about/strategy/people-and-culture

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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.