Teams at eGenesis

The QA Manager oversees GMP production operations, ensuring compliance with regulations and quality standards in manufacturing drug products.

Lead and execute environmental monitoring for GMP manufacturing sites: collect and process air/surface samples, document results, trend data, manage deviations, author and review QC records, and support contamination control and cross-functional cleaning/gowning programs. Travel between Wisconsin and Indiana (~20%).

The Senior Clinical Research Associate will manage clinical trial sites, ensure protocol compliance, data integrity, and oversee monitoring visits. Responsibilities include training site personnel, supporting patient recruitment, and ensuring inspection readiness.