Manager, Regulatory, International Markets (MENA) (1 year contract)

BridgeBio Pharma

Remote regions

Europe

Benefits

Job Description

This role supports submission of regulatory dossiers for international markets and ensuring all Module 1 administrative components and GMP registration requirements are met. The role requires documentation, review, and quality-checking administrative and technical documentation for new product registrations in MENA and other global regions. The role also needs the ability to track and maintain submission status, timelines, and documentation in relevant systems to support efficient registration processes. Strong proficiency with Veeva Vault RIM for document management is necessary. Must understand country-specific regulatory expectations and submission processes outside the EU and US. Effective communication and collaboration skills across cross-functional and global teams is needed.

About BridgeBio Pharma

BridgeBio is a biopharmaceutical company dedicated to discovering, developing, and delivering transformative medicines for patients living with genetic diseases.

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