**Summary**:
Work in the Sterile Area for aseptic manufacturing in accordance with the GMP requirements, Novartis SOPs and production documentation. **About the Role**:
**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**: Learn about all the ways we’ll help you thrive personally and professionally.
- Read our handbook (PDF 30 MB) Division Operations Business Unit Production / Manufacturing Location Italy Site Saluggia Company / Legal Entity IT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl Functional Area Technical Operations Job Type Tempo pieno Employment Type Temporaneo (tempo determinato) Shift Work No

📌 Production Technician (Saluggia)
🏢 Novartis
📍 Saluggia