Grifols is seeking a Regulatory Affairs professional to prepare, review and manage CMC submissions and coordinate with Health Authorities across global sites. The role requires experience in RRAA within the pharmaceutical industry and a proactive approach to submission preparation.The position is based in Sant Cugat del Vallès with a hybrid work model, offering adaptable schedules and opportunities to interact with international regulators and affiliates.#J-18808-Ljbffr