Quality Documentation Specialist II – GMP/GLP (Columbus)

A leading Gene Therapy firm in Columbus, OH seeks a Quality Specialist II. This role focuses on quality documentation and the review of discrepancies in compliance with regulations. Candidates should have a Bachelor’s in a science-related field and 2-3 years of experience in heavily regulated labs. The role is fully onsite and offers a pay rate of $28/hr, with various benefits including medical, dental, and 401(k) plans. #J-18808-Ljbffr