20 beste vacatures voor de functie van regulatory affairs environment in brussels, bru (nieuwe medewerkers gezocht)

EU Regulatory Science Lead
UCB —Anderlecht
- Geneeskunde
Public Affairs and Patient Relations Manager
AbbVie —Waver
- Voltijds
- Hybride werken
Communications and Patients Engagement Officer VIE Contract
Sanofi —Diegem
- Marketing
- Master
- SharePoint
7 dagen
Senior Clinical Research Associate
BD —Erembodegem
- € 60.300 - € 91.950 per jaar
- Onderzoek
- Projectmanagement
- Bachelor
9 dagen
Graduate Intern, Financial Services Public Affairs Consultancy, 6-month paid internship
FleishmanHillard —Brussel
- Voltijds
- Financiële diensten
- Stage
- Taalopleiding voorzien
Sr Manager EMEA Advocacy & Regulatory Intelligence
Ansell —Brussel
- Voltijds
- ICT
- Communicatieve vaardigheden
- Onderhandelen
6 dagen
Project Manager Generalist | Life Science
Capgemini —Diegem
- PMP
- Projectmanagement
Quality Specialist
Hologic —Zaventem
- € 50.000 - € 70.000 per jaar
- ERP systemen
- Microsoft Office
- Bachelor
Health & Safety Adviser
IMA Europe —Brussel
- Voltijds
- Spaans
- Engels
- Ter plaatse
- GSM-vergoeding
- Pensioensparen
Snel solliciteren
8 dagen
Patient-Centered Outcomes Research (PCOR) Lead
UCB —Eigenbrakel
- Doctoraat
- Onderzoek
- Master
Medical Advisor, Cardiovascular (Belgium)
Abacus Medicine Group —Anderlecht
- Thuiswerk
- Geneeskunde
- Doctoraat
- Master
13 dagen
Drug Safety Advisor
Qplus consult —Melsbroek
- Doctoraat
- Master
EMEA GAPP Policy and Campaigns Executive, YouTube (English)
YouTube —Brussel
- € 106.000 - € 108.000 per jaar
- Bachelor
- Ter plaatse
6 dagen
EU Regulatory Strategy Team Lead
UCB —Anderlecht
- Doctoraat
- Master
Associate Consultant, Tech Policy
APCO Worldwide —Brussel
- Schrijfvaardigheden
- Projectmanagement
- Artificiële intelligentie
Project Manager Generalist | Life Science
Capgemini Sogeti —Diegem
- PMP
- Projectmanagement
Site Conformance Expert | Life Science
Capgemini Sogeti —Diegem
- € 50.000 per jaar
- Master
- Communicatieve vaardigheden
13 dagen
Site Conformance Expert | Life Science
Capgemini —Diegem
- € 50.000 per jaar
- Master
- Communicatieve vaardigheden
13 dagen
Digital Technology Lead Medical Affairs
UCB —Anderlecht
- Engels
- Master
DT Medical Affairs Lead
UCB —Anderlecht
- Master
- Bachelor

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs environment in brussels, bru

Door in te loggen op je account, ga je akkoord met de Algemene voorwaarden van SimplyHired en stem je in met ons Cookie- en privacybeleid.

Zoek vacatures in meer locaties

regulatory affairs environment jobs near brussels, bru

Vacatures voor een Communications Officer in Diegem

Vacatures voor een Stage Data Science in Brussels

Vacatures voor een Recruitment Consultant in Bruxelles

Vacatures voor een Vebego Cleaning & Services in Zaventem

Vacatures voor een Group Cleaning Services in Sint Lambrechts Woluwe

Vacatures voor een Advocacy Manager in Bruxelles Capitale

Vacatures voor een Cafe Manager in Brussel

Vacatures voor een Quality Specialist in Braine L'alleud

Vacatures voor een Food Technology in Bruxelles

Vacatures voor een Lead Architect in Bruxelles Schaarbeek

Vacatures voor een Technology Lead in Eigenbrakel

Vacatures voor een Chief Technology Officer in Ghent

Vacatures voor een Hr Officer in Hainaut

Vacatures voor een Communications Officer in Bruxelles

Vacatures voor een Communications Officer in Brabant Wallon

Vacatures voor een Communications Officer in Brussels

Vacatures voor een Payroll Officer in Brussel

Vacatures voor een Paid Intern in Brussels

Vacatures voor een Translation Intern in Bruxelles

Vacatures voor een Intern Politics in Zaventem

EU Regulatory Science Lead

UCB -
Anderlecht

Nu solliciteren

Vacaturegegevens

Vaste Jobs

Kwalificaties

Geneeskunde

Volledige vacaturetekst

Make your mark for patients

We are looking for an EU Regulatory Science Lead who is strategic, collaborative and adaptable to join our Global Regulatory Affairs team, based in our Brussels, Belgium offices.

About the role

You will drive the EU regulatory strategy and activities for assigned products across development, approval and lifecycle activities. You will be the main regulatory contact for EU health authority interactions, including the EMA where relevant. You will help shape practical plans, identify regulatory risks, and work with global and regional partners to support timely submissions and informed decision-making.

Who you will work with

You will work closely with the Global Regulatory Lead, EU affiliates, Global Regulatory Affairs colleagues, submission teams, and cross-functional partners across development, clinical, medical, safety, quality and commercial teams. You will also collaborate with EU health authorities and contribute regional insight into global regulatory planning.

What you will do

You will develop and implement EU regulatory strategies aligned with business objectives and global regulatory plans.

You will be responsible for coordinating EU submission activities in line with regulations, guidelines, timelines and agreed strategies.

You will manage EU regulatory risks by identifying options, recommending practical actions and supporting mitigation plans.

You will act as the key EU contact for assigned products, including EMA and national agency interactions where needed.

You will communicate clear regulatory plans, risks and updates to leadership, affiliates and cross-functional stakeholders.

You will maintain awareness of evolving EU regulations, guidelines, competitor activity and potential impact on product plans.

Interested? For this role, we are looking for the following education, experience, and skills:

You have a degree in life sciences, pharmacy, medicine, law or another relevant scientific or regulatory field.

You bring strong experience in EU regulatory affairs, including product development, marketing authorisations and lifecycle management.

You understand EU regulatory frameworks, procedures, health authority expectations and the evolving policy environment.

You can translate complex regulatory information into clear recommendations for different audiences.

You work well across functions, cultures and organisational boundaries, building alignment through evidence and credibility.

You are curious and aware about digital tools, data science and AI, and their potential impact on regulatory science.

You can adjust to changing conditions, learn quickly, and remain effective in evolving regulatory and scientific landscapes.

You are self-aware and looking for continuous learning and growth of self and others, by seeking and giving constructive feedback.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Nu solliciteren

Verfijn je zoekopdracht

regulatory affairs environment vacatures in brussels, bru

EU Regulatory Science Lead

Public Affairs and Patient Relations Manager

Communications and Patients Engagement Officer VIE Contract

Senior Clinical Research Associate

Graduate Intern, Financial Services Public Affairs Consultancy, 6-month paid internship

Sr Manager EMEA Advocacy & Regulatory Intelligence

Project Manager Generalist | Life Science

Quality Specialist

Health & Safety Adviser

Patient-Centered Outcomes Research (PCOR) Lead

Medical Advisor, Cardiovascular (Belgium)

Drug Safety Advisor

EMEA GAPP Policy and Campaigns Executive, YouTube (English)

EU Regulatory Strategy Team Lead

Associate Consultant, Tech Policy

Project Manager Generalist | Life Science

Site Conformance Expert | Life Science

Site Conformance Expert | Life Science

Digital Technology Lead Medical Affairs

DT Medical Affairs Lead

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs environment in brussels, bru

Related Searches

Zoek vacatures in meer locaties

Tools voor werkzoekenden

Werkgeverstools

Bladeren

Blijf verbonden