Experteer Overview
In this role you help ensure medicinal products and medical devices meet regulatory requirements. You will prepare and manage registration dossiers, coordinate submissions, and liaise with authorities to support approvals and renewals. You will stay current with regulations, coordinate translations, and collaborate with cross-functional partners to deliver timely, high-quality regulatory documents. This is an opportunity to contribute to Grifols’ mission as a general leader in plasma-derived medicines and improve patient outcomes.

Compensaciones / Beneficios
• Prepare, compile, and maintain registration dossiers and regulatory documentation for medicinal products and medical devices within the assigned portfolio.
• Prepare, review, and submit regulatory documentation for new registrations, renewals, variations, and other regulatory procedures.
• Review and validate dossiers prepared by other team members, ensuring accuracy, quality, and regulatory compliance.




• Monitor the progress of regulatory submissions and registration procedures, liaising with regulatory authorities when required.
• Maintain up-to-date knowledge of current regulations and regulatory requirements applicable to medicinal products and medical devices, ensuring ongoing compliance.
• Coordinate the translation of regulatory documentation, ensuring accuracy, consistency, and compliance with local market requirements.
• Collaborate with cross-functional teams and external partners to ensure timely and high-quality regulatory submissions.

Responsabilidades
• Bachelor's Degree in Health Sciences or engineering
• Experience in RRAA or technical departments within the pharmaceutical industry
• Analytical skills, attention to detail, and ability to summarize and evaluate
• Advanced level of Spanish and English (C1) and MS Office (Excel)

Requisitos principales
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📌 Regulatory Affairs Specialist (San Cugat del Vallés)
🏢 Grifols
📍 San Cugat del Vallés