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Medical Device Regulatory Specialist

Flemish Brabant Permanent 63,000€ - 77,000€ per year View Job Description
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.

Added 26/10/2026

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

About Our 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.

Job Description

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



The Successful Applicant

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



What's on Offer

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
Quote job ref
JN-102026-7134178

Job summary

Sector
Life Sciences
Sub Sector
Regulatory Affairs
Industry
Healthcare / Pharmaceutical
Location
Flemish Brabant
Contract Type
Permanent
Consultant name
Dries Driesen
Job Reference
JN-102026-7134178

Michael Page is an equal opportunity employer committed to workforce diversity, both as an employer as well as a recruitment service provider. Each recruitment decision we make for people we hire and people we place into new roles is based solely on the candidates’ knowledge, experience and skills.