Description
The role is a Puerto Rico-based scientific position responsible for independently conceiving, designing, implementing, and advancing scientific experiments; interpreting data; developing and executing validation protocols, characterization studies, investigations, and change controls; and supporting aseptic drug manufacturing, process validation, technology transfer, and commercial process readiness. The position requires extensive pharmaceutical or biotechnology manufacturing experience, GMP and aseptic processing knowledge, statistical analysis, cross-functional collaboration, and strong scientific communication and project-management skills. Education requirements include a doctorate with relevant postdoctoral experience, a master's degree with at least three years of relevant scientific experience, or a bachelor's degree with at least five years of relevant scientific experience.
