20 meilleures offres (it project manager, diegem, vlg) (à pourvoir)

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Regulatory Affairs Officer

Will Pharma SA
Wavre Bierges

Postuler rapidement

Détails de l'emploi

CDI | Temps plein
De 4 200 € à 4 800 € par mois

Avantages

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

Qualifications

Microsoft Word
Français
Microsoft Excel
Anglais
Bases de données
IT
Néerlandais

Description complète du poste

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)

Postuler rapidement

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Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : it project manager (diegem, vlg)

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