Maya Miatkowski, PMP, is an experienced professional in CMC regulatory and technical development with a strong background in the biotechnology sector. Currently serving as Manager, CMC Regulatory at Beam Therapeutics since January 2020, Maya contributes to strategic regulatory direction for genomic medicines and cell therapies, supports global regulatory submissions, and facilitates interactions with health authorities. Prior experience includes roles as Manager, Technical Development and Principal Research Associate at Beam, as well as Manufacturing Specialist II and Senior Associate Scientist at bluebird bio, where Maya led technology transfers and managed mRNA and lentiviral vector manufacturing. Maya also has a solid foundation in molecular diagnostics and research, with earlier positions at Partners HealthCare and Biogen, and holds dual bachelor's degrees in Forensic Science and Technology and Justice Studies from the University of New Hampshire.
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