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• Support the execution of Regulatory Strategy. Implement the regulatory strategy for assigned products by processing registrations, renewals, post‑approval changes, and promotional materials to obtain required health authorizations for business units.
• Ensure Complete Regulatory Submissions. Guarantee submission of complete dossiers to local health authorities through effective preparation and review processes to obtain timely approvals.
• Maintain Global Data Systems. Register product‑related information in global electronic systems (Veeva Vault RIM, Qualipso, 4M PromoMats, OnePack) to comply with Sanofi's global guidelines.
• Manage Documentation and Archives. Compile physical and electronic product dossier files by creating comprehensive backup documentation of all submissions to health authorities, ensuring compliance with corporate...