13 set - Saluggia
Novartis
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
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