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.

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 GMPenvironment.
• 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? 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.