Summary
About the Role
Major accountabilities:
· 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
· Collaborate with the Production Manager and the Qualified Person to the CAPA implementation for the production areas and processes
Minimum Requirements:
Work Experience: Previous experience in radiopharmaceutical companies is desirable.
Education: Scientific background
Languages :
- Fluent Italian
- Basic level 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? https://www.novartis.com/about/strategy/people-and-culture
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