Team Lead

Description

Led the qualification of a critical BioMérieux software project, pivotal in validating and releasing medical reagent batches at the end of the production chain.

Achievements

• • Ensured that differences between the new and old software’s calculations were not statistically significant, achieving compliance with regulatory standards and operational requirements.

• • Implemented cost-effective and low-risk strategies for internal validation, enabling the system’s successful deployment to production.