QA Glp Coordinator
il y a 1 semaine
- Rédige et/ou assiste au développement, à la révision, à l'implémentation de documents QA par rapport au GLP/GCLP ;
- Signe les protocoles et rapports d'études cliniques (dans le respect des procédures) ;
- Approuve tous les documents liés à la Bioanalyse au niveau QA ;
- Réalise des audits internes et défend le système qualité lors des audits externes ;
- Coordonne, dirige et assure le suivi des actions découlant des audits ;
- Interprétation de textes réglementaires GLP/GCLP : tient à jour son expertise et évalue l'impact des changements réglementaires sur nos procédures ;
- Conseille et s'assure que les employés QA GLP/GCLP soient à jour au niveau de leur connaissance sur la législation et sur les procédures ;
- Donne des formations concernant la qualité aux collaborateurs de Bioanalyse.
**Votre profil**
- Diplôme: Master en chimie ou biochimie ou similaire avec une connaissance experte des procédures et des principes GLP et GCP ;
- Expérience professionnelle préalable de 2 ou 3 ans minimum ;
- Qualités: rigoureux, enthousiaste, créatif, flexible, polyvalent, esprit d'équipe ;
- Respect des instructions de travail ;
- Langues: français + anglais scientifique parlé et écrit ;
- Informatique: connaissance de Microsoft Office.
**Notre offre**
- Contrat à durée indéterminée
- Temps plein
- 12 jours de RTT par an
- Salaire brut + Chèques-repas 8€ + assurance groupe + assurance hospitalisation (à tarif réduit)
- Abonnement SNCB remboursé intégralement (trajet domicile-travail)
- Leasing vélo
Type d'emploi : Temps Plein, CDI
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