ppWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a general healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce, and market innovative medicines, solutions, and services in more than 110 countries and regions. /p h3Mission /h3 pThe RRAA Specialist will be responsible for the preparation of technical documentation, submission and following up of product registration and/or renewal, variations dossiers, as well as other regulatory documentation. /p h3Responsibilities /h3 ul liPrepare, compile, and maintain registration dossiers and other regulatory documentation for medicinal products and medical devices within the assigned portfolio. /li liPrepare, review, and submit regulatory documentation for new registrations, renewals, variations, and other regulatory procedures. /li liReview and validate dossiers prepared by other team members, ensuring accuracy, quality, and regulatory compliance. /li liMonitor the progress of regulatory submissions and registration procedures, liaising with regulatory authorities when required.



/li liMaintain up‑to‑date knowledge of current regulations and regulatory requirements applicable to medicinal products and medical devices, ensuring ongoing compliance. /li liCoordinate the translation of regulatory documentation, ensuring accuracy, consistency, and compliance with local market requirements. /li liCollaborate with cross‑functional teams and external partners to ensure timely and high‑quality regulatory submissions. /li /ul h3Qualifications /h3 ul liBo thorn the necessary bachelor's degree in Health Sciences or engineering. /li liExperience in RRAA or technical departments within the pharmaceutical industry. /li liAnalytical skills, attention to detail, and ability to summarize and evaluate. /li liAdvanced level of Spanish and English (C1) and proficiency in MS Office (Excel). /li /ul h3Benefits /h3 ul liHybrid Model: Flexible remote/on‑site schedule. /li liFlexible schedule: Monday–Thursday 7–10 to 16–19h and Friday 8–15h. /li liPermanent position. /li liLocation: Sant Cugat del Vallès, Spain. /li /ul pWe believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please let us know. Grifols is an equal opportunity employer. /p /p #J-18808-Ljbffr

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