Eurofins USA BioPharma Services seeks a qualified supervisor to oversee regulatory studies, ensure GLP compliance, and interpret data. You will assist in protocol development, design, and reporting while supervising scientific staff. Position is full-time, Monday–Friday, with overtime as needed.
Minimum 5 years of experience in biocompatibility studies and a BS degree in a related field are required; strong regulatory knowledge of EPA, FDA, DOT, OECD, and ISO standards is essential.
#J-18808-LjbffrSenior GLP Study Director & Lab Lead in ten mile run at Unknown Company
This position is listed as full time and onsite.