# Associate Director, CMC Regulatory Science, International

Hiring organization: [Moderna](https://career.thegoodapps.co/organizations/moderna)

Canonical page: https://career.thegoodapps.co/jobs/59404fc2-d11e-44b2-8a4e-115fb86b6b5a

Listed on Moderna's own careers site. Applications go to them directly.

- Seniority: Senior

## Summary

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._

## 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

Apply on Moderna's site: https://modernatx.wd1.myworkdayjobs.com/en-US/M_tx/job/London---England/Associate-Director--CMC-Regulatory-Science--International_R19226