QA Lead, Genomic Medicine – Hybrid (Pharma)

A leading pharmaceutical company is seeking a Quality Assurance Associate II to support the quality oversight of GMP manufacturing for genomic medicines. This role requires a B.S. and 4 years of experience in a pharmaceutical environment with a focus on quality. Key responsibilities include reviewing GMP documentation and managing quality risks while maintaining strong partnerships with contract organizations. The position is hybrid, based in Framingham, MA, and offers involvement in external partner quality management. #J-18808-Ljbffr