QC Analyst II

Opportunity Overview

We are seeking a dedicated professional to enhance our quality department by supporting Good 'x' Practice (GxP) activities. This role plays a critical part in managing quality systems, implementing operational processes, and ensuring adherence to industry-leading quality standards.

Responsibilities

• Ensure compliance with current Standard Operating Procedures (SOPs), GxP-compliant documentation, and records within the quality management system.
• Conduct and evaluate analytical tasks in a pharmaceutical laboratory, including participation in shift work when necessary.
• Maintain the integrity of all quality assurance records and data, promoting collaboration between your team and other departments.
• Provide educational support and foster GxP knowledge among team members.
• Assist in quality audits and health authority inspections.

Essential Qualifications

• Proven experience in quality assurance with strong analytical skills.
• Proficiency with analytical technologies such as HPLC, GC, and titration.
• Familiarity with lab-specific software systems like Empower, Chromeleon, and TiAmo.
• Experience with GMP and strong technological expertise.
• Willingness to engage in shift work.
• Fluency in both German and English.

Commitment to Diversity and Inclusion

Our organization is dedicated to cultivating an outstanding, inclusive work environment with diverse teams that reflect the patients and communities we serve.

Why Join Us?

At Novartis, we believe that making a difference in the lives of people with diseases requires more than just innovative science; it takes a community of passionate individuals who collaborate, support, and inspire one another. If you're ready to contribute to creating a brighter future, we invite you to explore our mission further.

Benefits and Rewards

Discover all the ways we can support your personal and professional growth. Access our comprehensive benefits overview to learn more.