Regulatory Affairs Manager, CMC

Retro is seeking an experienced Regulatory Affairs professional to lead the strategy and operations for Chemistry, Manufacturing, and Controls (CMC) regulatory work across its pipeline of cell therapies, small molecules, and gene therapies. This onsite role in Redwood City involves developing global CMC regulatory plans, preparing submission dossiers, and serving as the primary liaison with health authorities like the FDA. The ideal candidate will bring over seven years of hands-on CMC regulatory experience, with a strong focus on cell therapy development and cross-functional collaboration.