GMP QA Documentation Specialist — Contract Role

A biotechnology firm is seeking a QA Documentation Specialist I for a 6-month contract in Bend, OR. The role includes responsibilities like managing GMP regulations, quality systems, and document tracking. Candidates should have strong communication skills and proficiency in Microsoft Office, especially Word and Excel. This position requires self-motivation and the ability to work in a fast-paced, multi-functional environment. #J-18808-Ljbffr