
Regulatory/CMC Contractor
- London
- Contract
- Full-time
- Lead regulatory interactions between global (US/EU/UK/Japan) and local MENA regulatory teams.
- Translate global dossier content into regionally aligned regulatory strategies.
- Guide deficiency responses, submission planning (Modules 1–5), and alignment with EMA/FDA standards.
- Provide strategic input on CMC documentation and local manufacturing/tech transfer projects.
- Support multiple active programs across vaccines, biologics, and small molecules.
- Collaborate with internal commercial teams to align regulatory and launch timelines.
- 10+ years in Regulatory Affairs with strong EMA/FDA exposure.
- Proven experience in vaccine registration and commercialisation.
- Understanding of global dossier development and regulatory gap assessments.
- Familiarity with in-licensing models and early-stage biotech collaboration.
- Strategic mindset with hands-on ability to manage ambiguity across regions.
- English fluency required; Arabic is a plus.
We are sorry but this recruiter does not accept applications from abroad.