Our partner is a clinical-stage biopharmaceutical company focused on improving the lives of patients with genetically defined diseases in areas of high unmet medical need, with an initial focus on rare diseases.

This critical hire ensured compliance with GxP and GMP regulations, developed quality systems, performed audits, and assessed risks in clinical trials and manufacturing. They ensured product safety and quality, assisted with inspections, and worked with teams to resolve quality issues and maintain regulatory compliance.