$224,900 – $404,600
Listed on Moderna’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
Lead a team of CMC regulatory experts at Moderna's Norwood site, developing and executing regulatory strategies for drug submissions across vaccines, oncology, and rare diseases. This director-level role requires deep expertise in pharmaceutical regulatory affairs, manufacturing, and quality to guide product portfolios through health authority approvals.
Our summary, not Moderna’s wording. The full posting is on their site.
What they ask for
Required
- MS or PhD in science or engineering discipline
- 10+ years pharmaceutical or biotech industry experience
- 8+ years in regulatory CMC including DMF/ASMF submissions
- Knowledge of US, EU, and ROW regulations
- Experience with CTD format and content for regulatory filings
- Strong written and oral communication skills
Nice to have
- MS or PhD in Molecular Biology, Pharmaceutics, Chemistry, or related field
- 10+ years in pharma/biotech with manufacturing or analytical focus
- 8+ years in biologics-focused regulatory CMC