Veronique Brusa

Veronique Brusa is a QA Specialist Analytical at KBI Biopharma since February 2022, responsible for reviewing and QA disposition of test data for cGMP-compliant drug substance samples. Prior experience includes a QA Specialist role at Sobi, where Veronique provided quality oversight for a bioanalytical laboratory and contributed to quality process improvements, CAPA management, and audits. As a QA Assistant at Light Chain Bioscience, responsibilities included supporting GCLP laboratory functions and managing quality documentation, while previous positions at Thermo Fisher Scientific and CEA involved technical roles in immunochemistry and biotechnology research. Veronique holds a Licence professionnelle in Métiers de la Biotechnologie and a Brevet de technicien supérieur in Bioanalyses et Contrôles.