MedTech Regulatory Lead — Global Compliance

Hace 6 días

Madrid, Community of Madrid, España BD Jornada completa
BD in Spain is seeking a Regulatory Affairs Specialist to guide regulatory activities across product development and commercialization. You will ensure compliance with MDR, prepare and maintain Technical Files, and manage international registrations in a fast-evolving global environment. Expect collaboration with cross-functional teams, audits by authorities, and contribution to product life-cycle regulatory tasks.