Healthcare Regulatory Coordinator

il y a 12 heures


Brussels, Belgique EuropaBio Temps plein

**Job Category**:
**European Union**

**Job Experience**:
**1 to 3 years**

**Job Location**:
**Brussels**

**Expiration Date**:
**25 Dec 2024**

**Healthcare Regulatory Coordinator**

Biotechnology is at the forefront of transformative, cutting-edge and research-intensive scientific advancements. Enabling wide-scale societal change, biotechnology underpins innovation to address and revolutionise how patients are treated and provide sustainable, resource-efficient, climate-friendly products and processes.

Biotechnology has unprecedented policy focus entering into the new Commission mandate and EuropaBio has the opportunity to deliver impactful regulatory frameworks for this globally strategic technology.

EuropaBio, the voice of Europe’s dynamic biotechnology industry, is currently seeking a motivated Regulatory Affairs coordinator to join the Healthcare Biotechnology Team for an indefinite period.

**The role includes**:

- Work closely alongside the Healthcare Team to create a complete service for impactful advocacy for biotechnology.
- Support the development of EuropaBio activities within the field of healthcare biotechnology and pharmaceutical regulation, representing member priorities
- Act as primary lead for the Regulatory Affairs Working Group and a sub-WG with a specific focus on the implementation of the Clinical Trials Regulation
- Act as liaison between members and the European Medicines Agency and European Commission
- Support regulatory aspects of other EuropaBio Healthcare Working Groups, including ATMPs and OMPs, plus the National Associations Council
- Support the implementation of EuropaBio strategy for healthcare advocacy, including translation of regulatory priorities into impactful activities,
- Support healthcare contribution into cross-cutting legislative development including the Biotech Act and other cross-sector initiatives

**Profile**
- Must have full permission to work in Belgium;
- Graduated in EU affairs and/or public health, science, regulatory affairs, political sciences, law or other area relevant to Healthcare Biotechnology;
- Must be a strong communicator and team player, able to work with EuropaBio teams to deliver high profile activities.
- Should have interest and experience with regulatory framework for medicines in Europe and preferable with experience working from an industry perspective, either directly or indirectly
- Proven practical knowledge of European and/or national policymaking, acquired during at least 1-2 years working experience in European Institutions and/or in a company, industry associations, or in consultancy firms, preferably with direct contact to European institutions and/or EU stakeholder;
- Will suit somebody interested in contributing to association development and activities across members and EuropaBio Councils
- Should have a desire to grow through working with the EuropaBio team to propose and help lead activities and representing the Association to potential Members
- Fluent written and spoken English (working language); additional EU languages a plus; Must have a very high standard of both written and spoken English (office language);
- Should be able to begin as soon as possible.

**Our commitment to you**
- Support for professional career development
- An engaging position, in a Healthcare team of 4 people, within a growing EuropaBio team of 12+ people
- Exposure to a fast growing industry at the centre of Europe’s transformation, and a key enabling technology for future medical and environmental innovation;
- Motivated colleagues and expert membership at the top of their field who readily impart knowledge and who work across teams;
- A comfortable central Brussels office space (combines closed and open plan) with an excellent view and an abundant supply of coffee and the occasional cake;
- Structured teleworking, combining home and office-based working;
- Generous benefits (see below)

**Terms and conditions**

At EuropaBio we value Work-life-balance. Staff well-being is of the utmost importance to us and we provide a great deal of flexibility to members of staff.

You will be offered a full time open-ended position (CDI), 40 hours/week.

Working hours are from 09:00 until 18:00 Monday - Friday.

In addition to 20 legal holidays, 12 RTT days and end-of-year closing.

Hospital, travel and group insurance.

Salary is 2700€ gross/month.

Meal vouchers of 8€/day worked;
Public transport costs;
Possibility to telework 2 days/week

Teleworking stipend.

**How to apply**

**Do not forget to mention that you found this job ad on the **Euractiv** Jobsite**



  • Brussels, Belgique Plasma Industries Belgium Temps plein

    **Function**: Coordinator global QA systems** Reporting to the Sr Supervisor Global QA Systems **Purpose**: As Coordinator global QA Systems **Accountabilities** As Coordinator global QA systems you will be part of the Global team internal oversight. The team consisting of colleagues in Belgium and The Netherlands is responsible for quality risk...

  • Regulatory Affairs Officer

    il y a 2 semaines


    Brussels, Belgique IQVIA Belux Temps plein

    Functieomschrijving – Regulatory Affairs Officer (RAO)Doel van de functieDe Regulatory Affairs Officer (RAO) is verantwoordelijk voor het uitvoeren van diverse Regulatory Affairs‑activiteiten binnen de farmaceutische omgeving. De focus ligt op het registreren, onderhouden en opvolgen van geneesmiddelen, het beheren van dossierwijzigingen en het...


  • Brussels, Belgique Osborne Clarke Temps plein

    **Who is Osborne Clarke?**: Osborne Clarke is an international full-service law firm with 26 offices in 13 different countries, spread over 3 continents with more than 2,220 lawyers and employees. Osborne Clarke opened its Brussels office 12 years ago and has rapidly grown into a full-service law firm counting more than 40 Belgian qualified lawyers,...

  • Medior Associate EU Regulatory

    il y a 2 semaines


    Brussels, Belgique Loyens & Loeff Temps plein

    ||Medior Associate EU Regulatory Medior Associate EU Regulatory Brussels 27 August 2025 As a leading firm, Loyens & Loeff is the logical choice as a legal and tax partner if you do business in or from the Netherlands, Belgium, Luxembourg or Switzerland, our home markets. Our clients can count on personal advice from any of our 900 advisers based in one of...

  • Kyc Coordinator

    il y a 12 heures


    Brussels, Belgique Oliver James Associates Temps plein

    Oliver James is looking for **_a KYC Coordinator for one of the most important bank in Europe. _**Do you already have some experience as AML analyst or KYC and you dream of being part of one of the largest banks in the country? Then, the person we want is you! **_Role Purpose_** *** The Analyst is responsible for conducting an onboarding review in line with...

  • Regulatory Submission Planner

    il y a 2 semaines


    Brussels, Belgique MSD Temps plein

    We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for...

  • Test Coordinator

    il y a 2 semaines


    Brussels, Belgique Contraste Europe Temps plein

    Join Contraste as a Test Coordinator.Location: Brussels, with 2 days remote work.Experience required: Minimum 3 years in test management or quality assurance.Languages required: French or Dutch + English.Scope: Ensure the quality and reliability of insurance products and services by overseeing testing processes within transformation projects.Contraste Europe...

  • Grid Integration Coordinator

    il y a 12 heures


    Brussels, Belgique Luminus Temps plein

    Publicatiedatum: 2 september 2024 - Brussels - Contract open-end Luminus' ambition is to remain No.1 in Wind Onshore generation. To reach this goal, Wind needs to improve its knowledge, processes and strategy for integrating renewable projects into the grid. Connecting our wind turbines to the grid, we often encounter problems with congestion or flexible...

  • Regulatory Affairs Officer

    il y a 12 heures


    Brussels, Belgique EG NVSA Temps plein

    **About EG** EG is the largest pharmaceutical company in Belgium. With an offering for just about every therapeutic area, we are the market leader in generic medicines and the biggest OTC company in Belgian pharmacies. We still produce many of our medicines and food supplements in Belgium. We currently have 180 employees and continue to invest in: - The...

  • Lead Engineer

    il y a 3 semaines


    Brussels, Belgique afarax Temps plein

    afarax is looking for a freelance Lead Engineer / Solution Designer - Risk – Compliance Regulatory Reporting. We need you!The project: Our client in the banking sector is looking for a Lead Engineer / Solution Designer - Risk – Compliance Regulatory Reporting to join their team.Mission:Understand the functional requirements of the projectDescribe the...