Medical Device Regulatory Specialist

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...

Michael Page Belgium is seeking a Regulatory Affairs Specialist for the medical devices sector to coordinate registrations across international markets and ensure MDR compliance. You will prepare and submit regulatory documentation, support lifecycle changes, and liaise with manufacturers, distributors and authorities.The role requires a Life Sciences or...

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...

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...

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...

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,...

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 —...

Materialise Belgium, part of Materialise Medical, seeks a highly qualified biocompatibility-focused engineer to drive validation and regulatory work for medical devices. You will work across cleaning, packaging, and sterilization processes, and support ISO 10993-1 assessments.You will collaborate with Quality, Regulatory, Development, Process Engineering,...

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...