$142,500 – $256,500
Listed on Moderna’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role manages regulatory chemistry, manufacturing, and controls (CMC) strategy and submissions for pharmaceutical products at Moderna, guiding cross-functional teams through clinical and commercial approval processes. It suits experienced pharmaceutical scientists and engineers ready to lead regulatory strategy work for biologics in a matrix organization.
Our summary, not Moderna’s wording. The full posting is on their site.
What they ask for
Required
- BS, MS, or PhD in Molecular Biology, Pharmaceutics, Chemistry, Chemical Engineering, or closely related field
- 8+ years in pharmaceutical or biotech industry with manufacturing and/or analytical focus
- 5+ years in biologics-focused regulatory CMC
- Knowledge of global CMC regulations and CTD format
- Experience with regulatory procedures for drug development, registration, line extensions, and license maintenance
- Ability to collaborate cross-functionally in a matrix environment
- Independent work capability
- Strong written and oral communication