GMP QA Specialist - Deviation & Docs (1 Yr)

A leading recruiting firm in the United States is seeking a QA Specialist with GMP experience to provide essential quality support in a pharmaceutical manufacturing environment. This on-site position focuses on quality assurance activities, particularly deviation management and GMP documentation. An ideal candidate will possess a Bachelor’s degree and 1 to 3 years of experience in a regulated pharmaceutical setting. This one-year contract role emphasizes compliance with GMP standards and documentation tasks. #J-18808-Ljbffr