Eurofins USA BioPharma Services in Dayton, NJ seeks a seasoned supervisor to oversee regulatory biocompatibility studies, develop and implement test protocols, and ensure GLP compliance across all study phases.
You will supervise technical staff, interpret data, write study reports, and liaise with sponsors and regulatory agencies while coordinating study schedules, budgets and resource needs.
#J-18808-LjbffrSenior GLP Study Director in south brunswick at Unknown Company
This position is listed as full time and onsite.