Save Job Back to Search Job Description Summary Similar Jobs Added 13/10/2026Drive medical device registrations across international marketsBroad RA exposure beyond dossiers, with strong stakeholder impactAbout 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 assigned international marketsPrepare and submit regulatory documentation with internal and external stakeholdersSupport ongoing compliance activities for medical device portfoliosManage regulatory aspects of product changes throughout the lifecycleReview and assess regulatory implications of marketing materialsMonitor regulatory developments and communicate relevant updatesAct as a key contact for manufacturers, distributors, and authoritiesContribute to continuous improvement initiatives within Regulatory AffairsThe Successful ApplicantAs a successful Regulatory Affairs Specialist - Medical Devices - EN, you will have the following profile:Bachelor's degree in Life Sciences, Biomedical Sciences, Pharmacy, Regulatory Affairs or related field1-3 years of experience in Regulatory Affairs within medical devicesStrong knowledge of MDR requirements and registration processesExperience supporting product registrations and lifecycle activitiesExcellent communication and stakeholder management skillsProactive personality who actively seeks information and drives actions forwardComfortable collaborating with international stakeholdersFluent in EnglishStrong analytical and organizational skillsTeam-oriented with a continuous improvement mindsetWhat's on OfferAs a successful Regulatory Affairs Specialist - Medical Devices - EN, you will have:Competitive salary package including extra-legal benefitsHybrid working modelInternational exposure within a global healthcare environmentStrong onboarding and development opportunitiesCollaborative culture with close interaction between Regulatory Affairs, Quality, and Clinical teamsOpportunity to build a long-term career in Regulatory AffairsContactMorgane DelgeyeQuote job refJN-092026-7115820Job summarySectorLife SciencesSub SectorRegulatory AffairsIndustryHealthcare / PharmaceuticalLocationFlemish BrabantContract TypePermanentConsultant nameMorgane DelgeyeJob ReferenceJN-092026-7115820
