The ideal candidate brings strong downstream biologics process expertise, significant GMP manufacturing experience, sound technical judgment, and the ability to partner effectively with CDMOs and internal Process Development, External Manufacturing, Quality, Regulatory, and Supply Chain teams. Bachelor’s, Master’s, or PhD in Chemical Engineering, Biochemical Engineering, Biotechnology, Biochemistry, or a related discipline, with relevant MSAT, process engineering, GMP manufacturing, technology transfer, or biologics manufacturing experience.