Key Responsibilities:

• Maintain compliance with current Standard Operating Procedures (SOPs), GxP-compliant documentation, and records within the Novartis quality management system.
• Perform and evaluate analytical tasks in a pharmaceutical laboratory, including working in shifts where necessary.
• Ensure the integrity of all quality assurance records and data, as applicable, and foster collaboration between your team and other functions and departments.
• Ensure an appropriate level of education and GxP knowledge.
• Support quality audits and health authority inspections.

Essential Requirements:

• Experience in quality assurance and analytical skills.
• Proficiency in analytical technologies (e.g., HPLC, GC, titration).
• Knowledge in the use of lab-specific software (e.g., Empower, Chromeleon, TiAmo).
• GMP experience and technological expertise.
• Willingness to work in shifts.
• Fluency in German and English.

This role is limited to 24 months.

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

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 / EEO: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.