Junior Regulatory Affairs Officer (Full-Time, Permanent)
Are you ready to take the next step in your regulatory affairs career and make a real impact on European health regulatory frameworks? AESGP is looking for a committed and driven Junior Regulatory Affairs Officer to strengthen our regulatory team and help advance the voice of the self-care industry in Europe.
Working with the AESGP team and members, you will be involved in regulatory and scientific policy development, providing input to evidence-based decision making, and contributing to the development of AESGP regulatory strategy.
This is a full-time, permanent role based in Brussels, offering hands-on engagement and a supporting role in developing AESGP’s interaction with European Union Institutions, regulatory bodies, and other stakeholders, fostering the Self-Care sector’s relationships with them.
Your KEY RESPONSIBILITIES will be:
- Monitor regulatory, policy and legislative developments at EU level and assess their impact on the self-care industry.
- Conduct research and develop industry positions, communications and presentations.
- Provide AESGP comments to consultations and regulatory guidance documents under preparation by relevant stakeholders.
- Develop and implement strategies to ensure regulatory approaches that support members’ interests.
- Provide regulatory and scientific advice to AESGP members.
- Coordinate internal members’ groups including preparation, moderation of the debate, building consensus and advising on possible regulatory strategies.
- Support in managing relations with AESGP members and external stakeholders.
- Accompany AESGP members at relevant stakeholder meetings.
- Attend and prepare for AESGP team meetings, committee meetings and expert group meetings.
- Carry out any other duties and projects appropriate to the post as required by the line managers.
Your required QUALIFICATIONS, EXPERIENCE and KNOWLEDGE should be:
- University degree in medical, biomedical, (bio)chemistry, pharmacy/pharmaceutical sciences, European Studies, Law or other science disciplines.
- Knowledge of the processes of the European Union as well as of legislative procedures.
- Knowledge of the European healthcare area (experience with general pharmaceutical legislation and medical devices regulation is an advantage).
- Understanding of the European Union political environment and political developments as they impact the Healthcare sector.
Your main SKILLS and ABILITIES should be:
- Good critical thinking and fact-finding skills, and ability to identify and understand key issues.
- Ability to present complex information in a concise manner in writing, presentations and oral communication.
- Detail-oriented with excellent organizational abilities.
- Able to prioritise and work under pressure, meeting deadlines with tight schedules.
- Being a team player with the ability to work independently and proactively.
- Excellent command of English, both oral and written, and another or more European Union languages.
- Good IT skills (Microsoft Office Suite); communication and design skills are a plus.
At AESGP we OFFER you:
- A full-time, permanent position in a respected Brussels-based association.
- Employment agreement of undetermined period (open-ended contract).
- A competitive salary package aligned with your experience and responsibilities.
- Meal vouchers, Hospitalisation insurance, Ambulatory care coverage and Pension fund.
- Mentorship from experienced industry professionals.
- Networking opportunities within the healthcare sector at the European and national levels.
- A supportive and collaborative work environment.
HOW TO APPLY
Interested candidates should send the following documents to info@aesgp.eu by 5th September:
- CV – in PDF, with the title “
– CV” - Cover letter – in PDF, with the title “
– Cover”
Please note that only shortlisted candidates will be contacted.