QC Analyst II

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.

We are looking for a dedicated QC Analyst to support Good 'x' Practice (GxP) activities in our quality department. This role involves managing quality systems, implementing operational processes and ensuring compliance with Novartis quality standards. This role is limited to 24 months.

• 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.