GLP Regulatory Study Director - Lab Lead

Eurofins USA BioPharma Services in Dayton, NJ seeks an experienced supervisor to oversee regulatory studies, ensure GLP compliance, and interpret data. You will develop protocols, train staff, and liaise with sponsors.

This role requires a BS degree, at least five years of biocompatibility study oversight, and strong knowledge of EPA, FDA, DOT, OECD, GLP, and ISO standards. Full-time with weekday hours and potential overtime.