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 oversees regulatory strategy and CMC submissions for mRNA medicines across global health authorities, requiring deep expertise in biologics regulation and manufacturing quality. It suits experienced pharmaceutical professionals with strong scientific credentials who can navigate complex regulatory pathways and lead cross-functional teams toward approval.
Our summary, not Moderna’s wording. The full posting is on their site.
What they ask for
Required
- Master's or PhD in Molecular Biology, Pharmaceutics, Chemistry, Chemical Engineering, or related field
- 10+ years in pharmaceutical or biotech industry with manufacturing or analytical focus
- 8+ years of biologics-focused regulatory CMC experience
Nice to have
- Experience in vaccines, oncology, or rare disease therapeutic areas
- Strong knowledge of EU and ROW regulations
- Strong knowledge of cGMP
- Strong experience with CTD format and regulatory filings
- Exceptional written and oral communication skills