QC Analyst II

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

Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, be-cause of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.