**Summary**:
Questo ruolo utilizza le competenze di laboratorio di chimica per testare e misurare prodotti o materiali, garantendo al contempo che l'analisi venga eseguita secondo le procedure operative standard (SOP), i metodi analitici e gli attuali compendi. **About the Role**:
**Key Responsibilities**: - Execute analyses on excipients, raw materials, pharmaceutical products, water, and primary and secondary packaging according to internal SOPs
- Perform stability studies, process validation protocols, method validation protocols and studies related to pharmaceutical products involved in technological transfer for the relevant sector
- Conduct qualifying tests for instrument performances - Properly record analyses in compliance with ALCOA+ principles
- Collaborate to achieve departmental goals
- Contribute to maintaining good conditions of laboratories, instruments and working environment
- Assist in keeping the Quality Control SOPs updated
- Review of GMP documentation **Essential Requirements**:



- Diploma/Degree in Chemistry
- Solid technical-scientific knowledge of pharmaceutical/chemical/QC/ or equivalent analysis
- Previous experience working in a laboratory environment in the pharmaceutical industry
- Experience in GMP environment
- Fluent in Italian and English **You will receive**: You can find everything you need to know about our benefits and rewards in the Novartis Life **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. Division Operations Business Unit Innovative Medicines Location Italy Site Saluggia Company / Legal Entity IT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl Functional Area Quality Job Type Tempo pieno Employment Type Temporaneo (tempo determinato) Shift Work No

📌 Qc Analyst (Saluggia)
🏢 Novartis
📍 Saluggia