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Solliciteren



regulatory affairs advisor


  • Location: Brussels, Belgium (Hybrid, 3 days/week on site, 2 days remote)
  • Type: Employee, full time
  • Duration: Permanent contract
  • Starting date: January 2026
Tasks

ABOUT THE ROLE

We are seeking a Regulatory affairs Advisor with strong interest in EU health policy, to join our dynamic and multicultural team in Brussels.

Key Responsibilities

  • As part of the Public Affairs team, you will work towards influencing positive evolution of regulatory requirements and supporting members in achieving compliance.
  • In the coming years, the EU Good Distribution Practice (GDP) Guidelines - governing how medicinal products are handled, stored, and distributed across the EU - will undergo a significant transformation into binding legislation. You will be spearheading this work on behalf of GIRP.
  • As the leading European association representing GDP-inspected entities, GIRP offers you the opportunity to make a real impact—ensuring that patients across the EU continue to receive safe, high-quality, and properly controlled access to medicines.

Main tasks include:

  • Monitor upcoming relevant healthcare legislative and policy developments
  • Analyse impact of EU health-related legislative and policy developments on the pharmaceutical wholesale sector
  • Lead the discussions on the revision of the Good Distribution Practice Guidelines with EMA, the European Commission and supply chain stakeholders
  • Coordinate our legal and regulatory experts' contributions
  • Participate in events and external working groups of relevance
  • Support advocacy and stakeholder engagement activities
Requirements

Required Qualifications

  • Master's degree in regulatory affairs or law
  • 3 to 4 years of professional experience in EU regulatory affairs
  • Understanding of EU institutions and legislative processes
  • Native-level proficiency in English
  • Strong interest in health policy and regulatory affairs
  • Organised, analytical, and a proactive team player
  • EU national or EU work visa handler

Desirable Qualifications

  • Understanding of the dynamics of pharmaceutical supply chain
  • Knowledge of the EU Good Distribution Practice Guidelines
  • Experience in advocacy for healthcare, policy, or European affairs
Benefits

WHY JOIN US?

  • You'll have the opportunity to make a real impact on the future of pharmaceutical wholesale in Europe, especially the revision of the GDP.
  • You'll be part of a dynamic multicultural team in a pivotal moment of transformation.
  • You'll work alongside passionate professionals who are committed to making a difference.
  • GIRP is an equal opportunity employer, committed to diversity and inclusion.
  • We promote a safe, respectful, and healthy work environment.
  • We actively support the physical and mental well-being of everyone on our team.

HOW TO APPLY

  • Send your CV, cover letter and net monthly salary expectation
  • Deadline: 15 November 2025
  • Only shortlisted candidates will be contacted

Solliciteren

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