Regulatory Affairs Spain

Experteer OverviewIn this role you monitor global regulatory developments for medicinal products and medical devices, ensuring accurate country-specific content within an AI-assisted editorial environment. You contribute to a cross-border Regulatory Intelligence team that shapes a comprehensive regulatory resource for the pharma and medical devices industry. You will analyze regulatory updates, apply editorial standards, and publish harmonised content to support drug development and market access. This position offers meaningful impact through data-driven regulatory insights and collaboration across diverse teams.
Compensaciones / Beneficios- Monitor and collect regulatory information from identified sources and publish regulatory documents following CRI scope and editorial processes- Gather and analyse scientific, regulatory, and industry data to support a comprehensive industry resource- Contribute to development of regulatory content for assigned countries within the team- Crea...