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Sarepta is at the forefront of genetic medicine, particularly in the treatment of Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs). With over 40 programs in various stages of development, including gene therapy, RNA, and gene editing, Sarepta launched its fourth therapy in 2023, marking a significant milestone as the first-ever gene therapy for Duchenne. The Senior Director overseeing internal Quality Control Testing will lead a team of approximately 50 QC analysts, managing an integrated testing schedule that supports both late-phase commercial manufacturing and early-phase clinical pipelines. This role is crucial in ensuring a continuous global supply of Sarepta's AAV gene therapies for neuromuscular disorders, requiring collaboration with Manufacturing, Quality Assurance, and Regulatory Affairs departments.