Regulatory Policy Officer (Digitalisation & New Technologies)

Euractiv; Brussel Hoofdstad; Sur place; EUR 50 000 - 70 000; Plein temps

Avantages offerts par ce poste

Meal vouchers

Remote work allowance

Hospitalisation insurance

Pension fund

Résumé du poste

Euractiv is looking for a Regulatory Policy Officer based in Brussels to manage European regulatory initiatives with a focus on new technologies, digital health, and AI.

This full-time position offers the possibility of a long-term contract and includes various benefits such as meal vouchers, remote work allowance, and health insurance. Ideal candidates will have a Master's degree and experience in health policy.

Applications are open until June 8, 2026, with early submissions encouraged.

Qualifications

• 2+ years of experience in European health/pharmaceutical policy or advocacy.
• Proficient in English; knowledge of EU languages is an asset.
• Experience advocating towards decision makers.

Responsabilités

• Monitor and advise on regulatory and policy areas.
• Engage in the implementation of revised Pharmaceutical legislation.
• Represent Medicines for Europe and advocate on its behalf.

Connaissances

Project management skills

Communication skills

Strategic thinking

Advocacy skills

Formation

Master’s degree in health policy, law, or similar

Outils

IT tools for marketing authorisation processes

Description du poste

About the Role

The Regulatory Policy Officer will manage essential European regulatory and policy initiatives and projects with a key emphasis on new technologies and telementic tools, digital regulatory infrastructure and systems, electronic product information, use of AI, and digital health strategies.

They will interact with membership and external partners including health authorities and EU institutions and support the Medicines for Europe Team for projects and events, including the implementation of the revised Pharmaceutical Legislation.

Reporting to the Executive Director, Regulatory & Scientific Affairs, the Regulatory Policy Officer will:

• Monitor, analyse and advise on a number of regulatory and policy areas related to electronic product information, telematic tools, digital regulatory infrastructure, digital health strategy and AI.
• Engage in the implementation process of the revised Pharmaceutical legislation.
• Research and monitor policy developments and key topics in support of the broader regulatory & science strategy of Medicines for Europe.
• Coordinate the corresponding internal committee, working groups and task forces, including drafting of agendas, minutes, reports and briefing notes, as well as data collection.
• Represent Medicines for Europe and advocate on its behalf on these issues towards the relevant external decision makers and other stakeholders such as the European Commission, National Competent Authorities, EMA and others.
• Liaise & collaborate with other European industry trade associations and other stakeholders on common policy issues on behalf of Medicines for Europe.
• Inform & support other Medicines for Europe sector groups, committees and working groups on horizontal issues.
• Provide feedback to the Executive and Board on the issues indicated above, as appropriate.
• Support the organisation and programme development of conferences (events, sessions, workshops) on key advocacy topics.
• Develop the response to external public consultations (e.g. draft guidelines), produce position papers and communications, develop and conduct surveys amongst different working groups and inform association members of developments in the areas indicated above.
• Contribute to the development of communication and educational materials as needed.

About your Profile

• A Master’s degree in a relevant field, either in health policy, law, or in medical/healthcare science, pharmaceutics and similar.
• At least 2 years’ experience in European health/pharmaceutical policy, pharmaceutical industry, advocacy groups, regulatory authority or in any other organisation dealing with the above areas.
• Knowledge of marketing authorisation regulatory processes and the IT tools supporting them will be an advantage.
• Experience in advocating towards decision makers would be an asset.
• Written and spoken proficiency in English with a knowledge of additional EU languages is an asset.
• Excellent project management skills including ability to handle multiple parallel projects and flexibility to adapt and reprioritise time sensitive issues.
• Dynamic, entrepreneurial (proactive & autonomous) and high self‑motivated personality with a “can‑do” mentality.
• Strong communication, writing and presentation skills.
• Comfortable in a multicultural environment.
• Strategic thinking and creativity to convey complex ideas clearly.
• A valid EU work permit.

About the Offer

• The opportunity to impact the lives of millions of patients and consumers, as well as the functioning of an entire sector of the European economy with your work and problem‑solving skills.
• Full‑time position: a one‑year contract with the potential to turn it into an indeterminate one.
• A salary package including meal vouchers (8€ per working day), a net remote work allowance, hospitalisation insurance (+ ambulatory) and pension fund.
• The possibility to represent a dynamic European industry and interact with diverse stakeholders and an extensive level of external exposure.
• Regular European travel.
• The opportunity to take ownership and have impact as well as being part of a motivated and multicultural team.

The deadline to apply is 8 th June 2026 at 23:59 with early applications to be encouraged.