Leah Evers

Leah Evers is a seasoned professional in quality assurance and regulatory affairs, currently serving as Quality Assurance/Regulatory Affairs Manager for In Vitro Diagnostics (IVD) at PathoFinder B.V. since March 2022, responsible for maintaining ISO 13485 and IVDR 2017/746 certified QMS. Prior to this role, Leah Evers held various positions, including Quality Assurance Officer and Manager at Medace BV, where the focus was on optimizing quality systems to expedite the market entry of medical devices. Leah Evers also contributed to quality assurance efforts at Chemelot InSciTe and previously worked as a technician involved in the development of PCR kits at PathoFinder B.V. and performed clinical analysis in earlier roles at Orbis medisch en zorgconcern and academic institutions. Leah Evers holds a Bachelor of Applied Science in Life Science from Fontys University of Applied Sciences.