Manager, Regulatory, International Markets (MENA) (1 year contract)
BridgeBio Pharma(1 month ago)
About this role
A Regulatory Affairs role supporting international product registrations and submissions to enable market access across global regions, with emphasis on MENA territories. The position works closely with cross-functional subject-matter experts and regulatory authorities to ensure compliance with country-specific requirements. It also involves maintaining regulatory records and systems to support efficient submission and lifecycle management.
Required Skills
- Regulatory Dossiers
- Module 1
- GMP Registration
- Documentation Review
- Veeva Vault
- Metadata Management
- Workflow Routing
- Stakeholder Collaboration
- Submission Tracking
- Agency Responses
+2 more
Qualifications
- Bachelor's Degree in Life Sciences, Pharmacy or Regulatory Affairs
- Master's Degree Preferred
About BridgeBio Pharma
bridgebio.comBridgeBio is a biotechnology company designing transformative medicines for patients with genetic diseases and cancers driven by clear genetic causes. The company advances programs from target discovery through clinical development, combining human genetics and translational science with rigorous clinical trials to create targeted therapeutics. BridgeBio builds a diversified portfolio of wholly owned and partnered programs across multiple modalities and uses a venture‑style operating model to accelerate and de‑risk development. Its mission is to translate genetic insights into precision medicines for patients with high unmet medical need.
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