Published: 06 March 2024
Basel
100%
Permanent position
About the Role
Your key responsibilities:
Your responsibilities include, but are not limited to:
• 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 on several tasks (management of material stocks, training of new personnel and CAPA implementation for the production areas and processes
Diversity & Inclusion / EEO
Role Requirements
• Scientific background.
• Proficient in Italian. Basic knowledge of English.
• Previous experience in pharmaceutical companies is desirable.
Work location: Ivrea.
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? https://www.novartis.com/about/strategy/people-and-culture
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