About this role
Consultant 2 at Eliquent Life Sciences. Location: Columbus, Ohio, United States. Role: developing plans, designing approaches, authoring protocols Requirements: 3+ years pharmaceutical/biotech/device/regulatory manufacturing experience, 2+ years cleaning validation, experience authoring validation documents, HBEL/ADE/PDE/MACO calculations, and toxicological assessments. Category: Communications and Public Affairs Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English