Biologics GMP Documentation Specialist - Audit-Ready

Meet Life Sciences is seeking a GMP Documentation Specialist in San Antonio, Texas. This project-based role involves creating and reviewing GMP documentation for biologics manufacturing. Candidates should have a Bachelor’s in Life Sciences and at least 3 years of GMP documentation experience in regulated environments. The position requires attention to detail and familiarity with cGMP standards. Preferred experience includes exposure to regulatory inspections and working with document management systems like Veeva or MasterControl. #J-18808-Ljbffr