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Medical Device Regulatory Specialist

Brabant flamand Permanent 63,000€ - 77,000€ par an Voir la description du poste
As a Regulatory Affairs Specialist, Medical Devices you will coordinate medical device registrations and support ongoing regulatory compliance across different markets.The position covers more than dossier preparation. You will also manage regulatory activities throughout the product lifecycle, assess product changes and follow new developments within medical device regulations.

Mise à jour 26/10/2026

  • Regulatory Affairs, Medical Devices, MDR, EU MDR, Product Registration
  • Product Lifecycle Management, Change Control, Regulatory Intelligence

À propos de notre client

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 Affairs Specialist who will work closely with Quality, Clinical Affairs and other international stakeholders.

Description du poste

As a Regulatory Affairs Specialist, Medical Devices your responsibilities are:

    • Coordinate medical device registrations across assigned international markets
    • Prepare, review and submit regulatory documentation with internal and external stakeholders
    • Support regulatory compliance and manage changes throughout the product lifecycle
    • Review marketing materials and assess their regulatory implications
    • Monitor regulatory developments and communicate relevant updates internally
    • Act as a contact for manufacturers, distributors and competent authorities



Profil recherché

A successful 'Regulatory Affairs Specialist, Medical Devices' should have:

    • Bachelor's or master's degree in Life Sciences, Biomedical Sciences, Pharmacy, Regulatory Affairs or a related field
    • Between 1 and 3 years of Regulatory Affairs experience within medical devices
    • Good knowledge of MDR, product registrations and regulatory documentation
    • Proactive and organised, with strong analytical and communication skills
    • Comfortable working with international teams and different stakeholders
    • Fluent in English



Conditions et Avantages

Our customer offers you:

    • A permanent contract with a competitive salary package
    • Attractive extra-legal benefits
    • International exposure within the medical device industry
    • Structured onboarding and development opportunities
    • The possibility to build a long-term career in Regulatory Affairs

If you would like to use your regulatory knowledge in the Life Science industry, please apply.

Contact
Dries Driesen
Indiquer la référence de l'offre
JN-102026-7134178

Résumé du poste

Secteur
Sciences de la vie
Sous-secteur
Qualité/Affaires Réglementaires
Industrie
Healthcare / Pharmaceutical
Où ?
Brabant flamand
Type de contrat
Permanent
Nom du consultant
Dries Driesen
Référence de l´offre
JN-102026-7134178

Michael Page s’engage pour l’égalité des chances, en tant qu’employeur ainsi qu’en tant que partenaire pour le recrutement. Toutes les décisions de recrutement que nous prenons sont basées uniquement sur l’expérience et les aptitudes de nos candidat(e)s.