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

Posted about 1 month agoViewed
UK, NetherlandsContractBiopharmaceutical
Company:BridgeBio Pharma
Location:UK, Netherlands
Languages:English
Seniority level:Manager, 5-10 years
Experience:5-10 years
Skills:
Project ManagementProject CoordinationDocumentationAttention to detailOrganizational skillsComplianceCross-functional collaboration
Requirements:
5–10 years of experience preparing and compiling regulatory dossiers for international markets Proven experience supporting registrations in MENA regions and other global territories Strong proficiency with Veeva Vault RIM for document management, workflow execution, and metadata accuracy Solid understanding of country-specific regulatory expectations and submission processes outside the EU and US Bachelor’s degree in Life Sciences, Pharmacy, Regulatory Affairs, or related discipline (Master’s preferred) Excellent organizational skills with strong attention to detail Ability to manage multiple concurrent submissions Effective communication and collaboration skills
Responsibilities:
Prepare, compile, and support submission of regulatory dossiers for international markets Coordinate, review, and quality-check administrative and technical documentation for new product registrations in MENA and other global regions Manage regulatory documents and data within Veeva Vault RIM Work closely with SMEs to gather required documentation as per country-specific regulations Track and maintain submission status, timelines, and documentation Support preparation of responses to agency queries Maintain organized records of international regulatory submissions and lifecycle documents
About the Company
BridgeBio Pharma
View Company Profile
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