Global Medical Devices Regulatory Affairs Specialist

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

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...

Michael Page zoekt een Regulatory Affairs Specialist, Medical Devices, ter versterking van zijn Regulatory Affairs team. Je werkt nauw samen met Quality, Clinical Affairs en internationale stakeholders.Je registreert medische apparaten in toegewezen markten, bereidt en dient regulatory documenten in, en bewaakt regulatory compliance gedurende de...

Michael Page is seeking a Regulatory Affairs Specialist for Medical Devices (EN) to coordinate international registrations, prepare regulatory submissions, and maintain lifecycle compliance. The role involves liaising with manufacturers, distributors, and authorities, and ensuring alignment with MDR requirements.The successful candidate will have 1–3 years...

Wat: Frequentie: Dagelijks Wekelijks Our client is an international healthcare organisation active in the medical device industry. The company develops and distributes products that support healthcare professionals and patient care across several international markets. To strengthen its Regulatory Affairs team, the organisation is looking for a Regulatory...

Regulatory Affairs, Medical Devices, MDR, EU MDR, Product RegistrationProduct Lifecycle Management, Change Control, Regulatory IntelligenceAbout Our ClientOur client is an international healthcare organisation active in the medical device industry. The company develops and distributes products that support healthcare professionals and patient care across...

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...

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 —...

Medical Affairs Manager Cardiovascular EMEADatum: 28.10.2026Kategorie: Clinical & MedicalDepartment InfoThe Medical & Clinical Division (M&C) plays a key role in demonstrating how our products and solutions can benefit patients. We generate and translate clinical evidence, collaborate with physicians and scientific experts, support scientific publications,...