The incumbent participates in the implementation and maintenance of the quality management system (QMS), with a focus on one or more program areas, including collection of blood and cellular therapy products, manufacturing and distribution, clinical services, transfusion services, laboratory services, and clinical research, as well as organization-wide support functions such as information systems, facilities, and safety. Minimum two years relevant experience includes any combination of: specialized experience as a quality professional, preferably in a healthcare or drugs/biologics/medical devices manufacturing setting, or clinical or technical work performed in a healthcare, laboratory, or drugs/biologics/medical devices manufacturing setting.