REGULATORY AFFAIRS ADVISOR
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Job Location:
Monthly Salary:
Posted on:
29 days ago
Vacancies:
1 Vacancy
Job Summary
- 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 impactensuring 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
- Masters 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
- Youll have the opportunity to make a real impact on the future of pharmaceutical wholesale in Europe especially the revision of the GDP.
- Youll be part of a dynamic multicultural team in a pivotal moment of transformation.
- Youll 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
Key Skills
- Proofreading
- Adobe Acrobat
- FDA Regulations
- Manufacturing & Controls
- Biotechnology
- Clinical Trials
- Research & Development
- GLP
- cGMP
- Product Development
- Chemistry
- Writing Skills
About Company
GIRP the European Healthcare Distribution Association is a non-profit organization representing systemic wholesalers across Europe. We play a vital role in ensuring a reliable and efficient healthcare supply chain getting more than 62 million packs of medicines from more than 3500 man ... View more
