QA Documentation

Il y a 4 mois


Brussels, Belgique HAYS Temps plein

QA Documentation | Bruxelles | Intérim | Horaire de jour
**Votre nouvelle société**
Nous sommes activement à la recherche d’un **_QA Documentation_** pour l’un de nos clients actifs dans le secteur pharmaceutique situé à Bruxelles.
**Votre nouveau rôle**
En tant que **_QA Documentation_**, vous assurez la validation et l’approbation des documents analytiques tels que les dossiers de lot, fiches de spécifications, logbooks, certificats d’analyse et rapports d’analyse (émanant du laboratoire). Vous garantissez la conformité aux procédures locales et aux principes cGMP/ALCOA+, tout en veillant à l’intégrité des données générées. Vous soutenez la documentation des tests abandonnés/invalidés et des situations anormales. Vous suivez votre plan de formation, complétez vos évaluations de performance à temps et contribuez au suivi des indicateurs de performance (KPI). Enfin, vous incarnez les valeurs de l’entreprise telles que la diversité, l’inclusion, l’intégrité, l’excellence et le respect.

**Votre profil**
- Vous disposez d’un Master à orientation scientifique (ou équivalent par expérience).
- Le fait de justifier d’une première expérience professionnelle en qualité est un plus
- Vous parlez couramment le français et savez également communiquer en anglais
- Vous maitrisez les GMP et toutes autres règles relatives au domaine de la production pharmaceutique

**Que faire maintenant ?**
Cette offre d'emploi ne correspond pas totalement à vos attentes, mais vous cherchez un nouveau travail ? N'hésitez pas à nous contacter.
1104654
**Accreditation number**

**VG 292/BUOSA W.INT.35 W.SO.35**

**Brussels n° 00322-406-20121217


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