Competitive SalaryHybrid JobAcerca de nuestro cliente Medical devices multinational company Descripción Coordinate and assist in the preparation of technical documentation for use in regulatory submissions for product registrations, renewals, and registration changes.Maintain registration databases, product registration records, and key performance indicators, and communicate approved registrations.Follow company policies and procedures.Miscellaneous responsibilities as assigned.Perfil buscado (h/m) Bachelor's degree required (any field).Minimum 1-2 years of experience in Regulatory Affairs (MANDATORY).English Proficiency is required (B1).Experience in Pharmaceutical industries (MANDATORY).Knowledge and experience in Medical Devices is a plus.Basic computer skills, including Microsoft Office Suite.Ability to handle data in Excel.Qué Ofrecemos Competitive salary.Hybrid job.Be part of a multinational company. #J-18808-Ljbffr