Major Accountabilities:

• Perform analysis on excipients, drug substances, drug products, water and primary packaging according to internal SOPs 
• Execute stability study protocols, process validation protocols, method validation protocols and every study tied to drug products involved in technology transfer for the field of expertise 
• Perform the sterility test on the products from AAA sites  
• Perform instrument performance qualification tests whenever required 
• Register the analysis correctly and in compliance with ALCOA+ principles other than the relevant applicable SOPs 
• Collaborate with management for reaching the department objectives 
• Know and apply the relevant SOPs for the field of expertise 
• Collaborate in the maintenance of good conditions of laboratories, instruments and work environment 
• Collaborate in keeping quality control SOPs updated 

Obligatory requirements:

• Education: Master degree in Biology (or equivalent) or biology technical high school education.
• Languages: Basic knowledge of English, verbally and in writing
• Experiences: Previous experience in pharmaceutical companies is desirable 

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? http://www.novartis.com/about/strategy/people-and-culture

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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.