Key Responsibilities:

• Sample storage and management.
• Bioanalytical testing and documentation of API, drug substance, drug product, finished product, complaints, stability, packaging material samples.
• Ensure all activities are in compliance with cGxP, including data integrity.
• Stability: Testing storage and management and analytical documentation of stability samples to cGxP standards.

Essential Requirements:

• Previous experience working in a bioanalytical laboratory in QC environment in the pharmaceutical industry. Excellent expertise in bioanalytical techniques (cell splitting, bioassay and ELISA testing, etc).
• Completed apprenticeship as a laboratory assistant or equivalent training.
• Collaborative and result-oriented mindset.
• Strong administrative skills and GMP compliance.
• Efficient production and documentation of tasks.
• Proficiency in breakthrough analysis and resilience.

This role is limited for 12 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.

Accessibility and accommodation: