Study Manager Hplc
il y a 1 mois
Description de l'entreprise
**Rejoignez nos Laboratoires d’Excellence **
Avec plus de 61 000 collaborateurs dans 59 pays, Eurofins fournit des prestations d'analyses aux industries pharmaceutiques, alimentaires et dans le domaine de l'environnement. A la pointe des derniers développements en biotechnologie, en très forte croissance et leader dans son domaine d'activité, Eurofins est une société dynamique et ambitieuse avec la vision de devenir le leader mondial du marché de la bio-analyse. Rejoindre Eurofins c’est démarrer une expérience riche en challenges pour une carrière prometteuse.
La division BioPharma Product Testing constituée de 30 laboratoires sous environnement GMP renforce ses effectifs en France pour accompagner nos clients en fournissant nos services analytiques.
Au sein de notre laboratoire, nous recherchons pour notre site des Ulis (91) en CDI et à pourvoir dès que possible, un(e):
**STUDY MANAGER HPLC **(H/F)**
**CDI**
Description du poste
Directement rattaché(e) au Responsable de Laboratoire, votre expertise technique vous permettra de gérer les études analytiques de votre périmètre et d’assurer la communication auprès des clients.
Vous contribuerez ainsi à la satisfaction client, dans le respect des exigences des Bonnes Pratiques de Fabrication en vigueur (B.P.F), des cGMP (Good Manufacturing Practice) et du Code de la Santé Publique.
Vous serez chargé(e) de:
- Gérer les investigations analytiques du laboratoire : effectuer les investigations techniques, gérer la communication client associée, effectuer la revue des données, proposer des actions correctives,
- Etablir les faisabilités techniques et participer au chiffrage et au pré-design des projets,
- Etre l’interlocuteur direct des clients sur les problématiques analytiques,
- Etre back-up sur la gestion des projets de vérifications, transferts, validations, développements de méthodes,
- Etre back-up sur la rédaction des protocoles et rapports des projets,
- Etre le référent technique de votre service (apporter un support au laboratoire en cas de problématique analytique),
- Réaliser la vérification des documents de travail et la correction des données brutes,
- Gérer les évènements qualités,
- Rédiger les documents de travail (trames de rédaction et synoptiques),
- Mettre en place et suivre les actions d’amélioration continue du service,
- Respecter les délais de réalisation des actions conformément à la programmation établie,
- Contribuer à la préparation des visites clients (audits et visites commerciales),
- Participer aux réunions de suivi d’activités
**Qualifications**:
De formation Bac+3 minimum en chimie analytique, spécialisé en techniques chromatographiques (HPLC) sur les matières premières et produits finis. Vous justifiez d’une première expérience acquise sur un poste similaire en environnement GMP, idéalement en industrie pharmaceutique.
Excellent(e) communicant(e), sens du service client, force de proposition, vous aimez le travail en équipe et avez un excellent relationnel. Vous êtes autonome avec un esprit d’initiative, curieux et une bonne capacité d’adaptation aux constantes évolutions technologiques et réglementaires dans les domaines analytiques et cGxP.
Un bon niveau en Anglais est requis (clients à l’international, écrit, oral).
Vous souhaitez valoriser vos compétences dans une société dynamique offrant de réelles perspectives de carrière, alors rejoignez-nous
Informations supplémentaires
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