20 beste vacatures voor de functie van regulatory affairs manager in brussel (nieuwe medewerkers gezocht)

Regulatory Affairs Officer
Will Pharma SA —Wavre Bierges
- € 4.200 - € 4.800 per maand
- Voltijds
- Hybride werken
- Microsoft Word
- Microsoft Excel
- Engels
- Winstpremie
- Opleidingsvergoeding CE
Snel solliciteren
Head of Regulatory Affairs
Allianz —Brussel
- Voltijds
- Doctoraat
- Engels
- Financiën
1 dag
Manager Corporate Governance, Regulatory & Public Affairs
VBO FEB —Brussel
Auditor QA Pharmaco Vigilance | Brussel | 4 days/week
Plasma Industries Belgium —Brussel
- Microsoft Excel
- Microsoft Access
- Bachelor
Regulatory Affairs Manager
Nipro Europe Group Companies —Mechelen
- Management
- Teammanagement
- Communicatieve vaardigheden
Public Affairs and Patient Relations Manager
AbbVie —Waver
- Voltijds
- Hybride werken
10 dagen
Regulatory Affairs Manager
Nipro —Mechelen
- Management
- Teammanagement
- Communicatieve vaardigheden
Go To Market Manager for projects in Pharma & Life Sciences
PwC —Brussel
- Voltijds
- Hybride werken
- Verkoopervaring
- Engels
- Master
Global Regulatory CMC Scientist
UCB —Anderlecht
- Master
- Bachelor
- Communicatieve vaardigheden
Contract Manager Flexibility & Ancillary Services
Elia —Brussel
- Hybride werken
- Master
- Onderhandelen
REGULATORY AFFAIRS INTERNS - OBELIS SCHOOL OCTOBER 2026
Obelis Group —Brussel
- Microsoft Office
- Master
- Bachelor
2 dagen
Regulatory Affairs Specialist
Nipro —Mechelen
- Analytisch vermogen
- Bachelor
Patient-Centered Outcomes Research (PCOR) Lead
UCB —Eigenbrakel
- Doctoraat
- Onderzoek
- Master
10 dagen
Regulatory Affairs - Environment
Nipro —Mechelen
- Hybride werken
- Master
- Bachelor
- ICT
Corporate Affairs Executive
Imperial Brands —Brussel
- Microsoft Excel
- Onderzoek
Regulatory Affairs - Environment
Nipro Europe Group Companies —Mechelen
- Master
- Bachelor
- ICT
Regulatory Affairs Specialist
Nipro Europe Group Companies —Mechelen
- Analytisch vermogen
- Bachelor
Clinical Project Manager (IVD experience required)
Biocartis —Mechelen
- Voltijds
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Human Resources Intern, Public Affairs Consultancy, 6-month paid internship
FleishmanHillard —Brussel
- Microsoft Excel
- Microsoft Office
- Personeelszaken
- Taalopleiding voorzien
12 dagen
Medical Information & PV Officer
Chiesi Farmaceutici —Zaventem
- Bachelor
- Communicatieve vaardigheden
- Verpleegkunde

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Regulatory Affairs Officer

Will Pharma SA
Wavre Bierges

Snel solliciteren

Vacaturegegevens

Vaste Jobs | Voltijds
€ 4.200 - € 4.800 per maand

Extralegale voordelen

Winstpremie
Opleidingsvergoeding CE
Reiskosten vergoeding
Elektronische maaltijdcheques
Hospitalisatieverzekering
Thuiswerkopties
Bedrijfscomputer
Pensioensparen

Kwalificaties

Microsoft Word
Frans
Microsoft Excel
Engels
Databases
ICT
Nederlands

Volledige vacaturetekst

Are you passionate about Regulatory Affairs and looking for a role where collaboration and impact truly matter? Are you ready to grow within a dynamic, family-owned pharmaceutical company where quality and innovation are at the heart of everything we do? Then Will-Pharma could be the perfect place for you!

We are currently looking for a Regulatory Affairs Officer to strengthen our Regulatory Affairs team.

As Regulatory Affairs Officer, you will play an important role in supporting the lifecycle management of our product portfolio and ensuring regulatory compliance across several product categories. Your main responsibilities will include:

· Managing all artwork and text-related activities (PILs, labels, boxes, primary packaging materials) in close coordination with suppliers, project managers and internal stakeholders.

· Coordinating the proofreading process for mock-ups and ensuring accuracy, consistency and compliance.

· Updating and correcting product information documents, including SmPCs, labelling and PILs, in line with applicable changes and QRD guidelines prior to submission.

· Organising, coordinating and prioritising regulatory activities related to linguistic translations and reviews.

· Preparing, compiling and reviewing the regulatory sections of registration dossiers, in collaboration with the Regulatory Affairs Manager and, where required, external partners, in CTD and eCTD format.

· Preparing and submitting minor variations and notifications to support regulatory activities.

· Preparing and submitting notifications for food supplements.

· Reviewing and approving promotional materials related to food supplements and cosmetics, in accordance with the relevant legislation.

· Supporting the lifecycle management of the Will-Pharma product portfolio by applying regulatory processes and procedures and ensuring appropriate tracking of changes.

· Keeping up to date with current European and national legislation relating to medicinal products, medical devices, food supplements and cosmetics.

We are looking for someone who combines regulatory expertise with strong organisational skills and a collaborative mindset. You ideally have:

· A scientific degree.

· Practical experience in Regulatory Affairs, particularly in artwork and text management.

· Good knowledge of European regulatory requirements, mainly within the Benelux region.

· Excellent organisational and interpersonal skills, with strong written and verbal communication abilities.

· A structured, process-oriented approach and strong attention to detail.

· Good IT skills and the ability to quickly learn new software tools.

· A good understanding of regulatory tracking databases, MS Word, MS Excel and eCTD.

· Strong analytical and evaluation skills.

· Fluency in English, Dutch and French.

At Will-Pharma, you will join a medium family-owned company where people work together with passion, dedication and respect. We value quality, agility, personal relationships, collaboration and customer focus. We offer:

· A full-time, permanent position with a day schedule from Monday to Friday.

· A challenging and varied role with opportunities for personal growth and the development of in-depth product knowledge.

· The opportunity to develop yourself, take ownership and grow within a supportive environment.

· A competitive remuneration package, including fixed and variable components.

· Additional benefits such as hospitalisation insurance, group insurance and other fringe benefits.

· The opportunity to work in a wellbeing-oriented organisation, with initiatives designed to help employees stay healthy and continuously improve their wellbeing.

· A pleasant, diverse and multicultural working environment where collaboration and inclusion are highly valued.

Rémunération : 4 200,00€ à 4 800,00€ par mois

Avantages :

Assurance groupe
Assurance hospitalisation
Chèques repas
Formation continue
Indemnité kilométrique
Ordinateur de fonction
Participation aux bénéfices
Travail à domicile

Expérience:

Affaires réglementaires dans le secteur pharmaceutique: 2 ans (Requis)

Langue:

Anglais (Requis)

Lieu du poste : Travail hybride (1301 Wavre Bierges)

Snel solliciteren

Verfijn je zoekopdracht

regulatory affairs manager vacatures in brussel

Regulatory Affairs Officer

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Regulatory Affairs Manager

Go To Market Manager for projects in Pharma & Life Sciences

Global Regulatory CMC Scientist

Contract Manager Flexibility & Ancillary Services

REGULATORY AFFAIRS INTERNS - OBELIS SCHOOL OCTOBER 2026

Regulatory Affairs Specialist

Patient-Centered Outcomes Research (PCOR) Lead

Regulatory Affairs - Environment

Corporate Affairs Executive

Regulatory Affairs - Environment

Regulatory Affairs Specialist

Clinical Project Manager (IVD experience required)

Human Resources Intern, Public Affairs Consultancy, 6-month paid internship

Medical Information & PV Officer

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs manager in brussel

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