Regulatory Affairs Specialist, Medical Devices

About Our ClientInternational healthcare organization active in the medical device sector, supporting patient care through innovative products distributed across multiple global markets.Job DescriptionAs a successful Regulatory Affairs Specialist - Medical Devices - EN, you will have the following responsibilities:Coordinate product registrations across...

Jobat is seeking a Regulatory Affairs Specialist for an international healthcare organization active in the medical device sector. You will coordinate registrations across international markets and prepare regulatory documentation with internal and external stakeholders.You will support ongoing compliance activities, manage regulatory aspects of changes,...

Michael Page International Belgium est à la recherche d’un Regulatory Affairs Officer pour soutenir le développement et le maintien des autorisations réglementaires du portefeuille produits. Vous rejoignez une équipe spécialisée et contribuerez à la définition des stratégies d’enregistrement et au suivi des échanges avec les autorités.Le poste...

At Materialise Medical, we believe that better healthcare starts with solutions designed around the individual patient. If you’re passionate about bringing personalized care to every patient, you’ll love being a part of this team. Through the technology we develop, researchers, engineers, and clinicians are revolutionizing personalized treatment —...

Terumo Blood and Cell Technologies in Belgium seeks a Quality Manager to translate regulations into company policies, own the QMS areas, and drive continuous improvement.The role covers CAPA, nonconformities, document control, audits, and liaison with regulatory bodies; leadership of a team and cross-functional collaboration at Leuven.Candidates should have...

Materialise is seeking a seasoned Technical Portfolio Manager for CMF Standard to accelerate product development, streamline workflows, and reduce time-to-market across R&D, manufacturing, quality, and regulatory teams worldwide.The ideal candidate has 10+ years in CMF standard devices or regulated medical devices, with deep knowledge of ISO 13485, EU MDR,...

Materialise is seeking a Device Development Manager to lead engineers in designing and supporting personalized and standard medical devices, including 3D‑printed guides and implants. You will drive design transfer, validation, and lifecycle support while aligning with regulatory standards and quality practices.You will influence product development...

GC Corporation was founded in 1921 in Japan and has developed itself into one of the most prominent companies in the development, production and distribution of a very wide range of dental products. Since 1972 GC Europe NV, our European Headquarter is located at the Researchpark Haasrode in Leuven (Belgium). GC Europe NV supports and leads our different...

GC Europe NV is seeking a Scientific Affairs Specialist for the EMEA region. The role focuses on creating and communicating scientific information to support sales, product claims, and regulatory submissions, in collaboration with internal teams and external academics.The position requires a Master’s degree (PhD/DDS preferred), English fluency, strong...