20 beste vacatures voor de functie van pharmaceutical regulatory affairs in brussels (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
Regulatory Affairs - Environment
Nipro —Mechelen
- Hybride werken
- Master
- Bachelor
- ICT
Regulatory Affairs Specialist
Nipro —Mechelen
- Analytisch vermogen
- Bachelor
Regulatory Affairs - Environment
Nipro Europe Group Companies —Mechelen
- Master
- Bachelor
- ICT
Regulatory Affairs Specialist
Nipro Europe Group Companies —Mechelen
- Analytisch vermogen
- Bachelor
Global Regulatory CMC Scientist
UCB —Anderlecht
- Master
- Bachelor
- Communicatieve vaardigheden
Medical Information & PV Officer
Chiesi Farmaceutici —Zaventem
- Bachelor
- Communicatieve vaardigheden
- Verpleegkunde
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
Regulatory Affairs Manager
Nipro —Mechelen
- Management
- Teammanagement
- Communicatieve vaardigheden
EU Regulatory Strategy Team Lead
UCB —Anderlecht
- Doctoraat
- Master
5 dagen
Project Manager Generalist | Life Sciences
Capgemini —Diegem
- PMP
- Projectmanagement
Project Manager Generalist | Life Sciences
Capgemini Sogeti —Diegem
- PMP
- Projectmanagement
Medical Advisor Cardiorenal - Benelux
CSL Behring —Mechelen
- Voltijds
- Master
- Managementervaring
- Communicatieve vaardigheden
Junior Consultant - Pharma
IQVIA —Kampenhout
- Voltijds
- Master
- Communicatieve vaardigheden
Artwork & Packaging Development Expert (Belgium)
UCB —Eigenbrakel
- Master
- Projectmanagement
- Communicatieve vaardigheden
Clinical Project Manager (IVD experience required)
Biocartis —Mechelen
- Voltijds
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Medical Affairs Director UK & Ireland
Alfasigma Group —Mechelen
- ICT
- Managementervaring
Research Scientist II – Extractables & Leachables (E&L) Team Lead
Baxter —Eigenbrakel
- Onderzoek
- Managementervaring
- Communicatieve vaardigheden
- Opleidingsvergoeding CE
5 dagen
Director, International Policy Research and Economics
Bristol-Myers Squibb —Eigenbrakel
- Voltijds
- Hybride werken
- Microsoft Excel
- Onderzoek
- Ter plaatse

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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

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pharmaceutical regulatory affairs vacatures in brussels

Regulatory Affairs Officer

Regulatory Affairs - Environment

Regulatory Affairs Specialist

Regulatory Affairs - Environment

Regulatory Affairs Specialist

Global Regulatory CMC Scientist

Medical Information & PV Officer

Auditor QA Pharmaco Vigilance | Brussel | 4 days/week

Regulatory Affairs Manager

Regulatory Affairs Manager

EU Regulatory Strategy Team Lead

Project Manager Generalist | Life Sciences

Project Manager Generalist | Life Sciences

Medical Advisor Cardiorenal - Benelux

Junior Consultant - Pharma

Artwork & Packaging Development Expert (Belgium)

Clinical Project Manager (IVD experience required)

Medical Affairs Director UK & Ireland

Research Scientist II – Extractables & Leachables (E&L) Team Lead

Director, International Policy Research and Economics

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van pharmaceutical regulatory affairs in brussels

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