Teams at Moderna

The Associate Director leads a strategic partnership with the UK government, managing cross-functional teams and ensuring public health impacts through innovative mRNA solutions.

The Associate Director will oversee CMC regulatory strategies and submissions, ensuring compliance and quality across various therapeutic areas while leading regulatory discussions with health authorities.

Lead global CMC regulatory strategy and submissions for biologics, ensuring compliance with cGMP and international regulations. Oversee CMC documentation, provide regulatory guidance to manufacturing and quality teams, manage multiple programs, interact with health authorities, and improve CMC processes and templates to support product development across therapeutic areas.