Descrizione:
In this role you will be required to work in rotating shifts, including night turns.
Major Accountabilities
- Perform the analysis of batches following specific training;
- 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;
- Execute the calibration, verification, qualification and validation activities of the Quality Control processes and equipment;
- Responsible for the oversight on manufacturing for QC sampling activities.
- Raw Material and Finished Product testing, Environmental Monitoring and Sterility QC testing, and reporting of the QC results. Escalation in case of non-conformances and deviations and manage these quality incidents as per AAA procedures.
- Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow up and implementation, and Change Control management, including procedure and form revisions.
- Participation in assigned qualification/validation activities, as necessary.
- Prepares applicable documents, forms, and records such as analytical batch records and follows Good Documentation Practices.
- Support internal and external Audits and Inspections, as required.
Minimum Requirements
- Education: Chemical or biological degree is desirable.
- Previous experience in radiopharmaceutical companies is desirable
- Fluent Italian, good knowledge of English.
Benefits and rewards
Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
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.
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