Grifols is seeking an RRAA Specialist to prepare technical documentation, submit product registrations and renewals, and manage variations dossiers for medicinal products and medical devices.
You will review dossiers, monitor submission progress, coordinate translations, and stay current with regulatory requirements across the portfolio. The role is based in Sant Cugat del Vallès with a hybrid work model.
📌 Global Regulatory Affairs Specialist — Hybrid (España)
🏢 Grifols
📍 España
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