Grifols is seeking a Regulatory Affairs professional to prepare, review and manage CMC submissions and coordinate with Health Authorities across general sites.
Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil.
The role requires experience in RRAA within the pharmaceutical industry and a proactive approach to submission preparation. xhfqzwm
The position is based in Sant Cugat del Vallès with a hybrid work model, offering flexible schedules and opportunities to interact with international regulators and affiliates.