T3 Project Lead
Zeralda, Algeria Permanent Posted on Jan. 20, 2025 Closing on Jan. 30, 2025Mission :
T3 Project Leader est le garant d’études et Réalisation de projets d'investissement de bout en bout pour des projets jusqu'à 5 millions d'euros, afin d’atteindre les objectifs tracés par le site.
Activités principales :
- Respecter et Faire respecter les consignes de sécurité selon les guidelines HSE de SANOFI ainsi que les règles BPF.
- Fournir des informations sur les études de projets d'investissement, y compris la direction de chaque étape de l’examen, le soutien du site et le processus de prise de décision de M&S.
- Réalisation de projets d'investissement de bout en bout pour des projets jusqu'à 5 millions d’euros, y compris le lancement, la conception, l'exécution, le C&Q, la remise et la clôture.
- Rapport mensuel sur les projets d'investissement concernant tous les indicateurs clés de performance du projet en matière de sécurité, de coûts, de calendrier et de ressources.
- Respect de toutes les normes et politiques obligatoires de conformité de Sanofi, locales et réglementaires, y compris les GMR de sécurité de la construction, les normes Planet Care, les BPF et les réglementation /normes de la FDA.
- Favoriser une culture de la sécurité avant tout et de la qualité tout au long du projet en mettant en œuvre les méthodes de travail SMS 2.0 et TRT.
- Assurer la dotation en personnel de toutes les ressources du projet d'ingénierie et aligner le plan stratégique de main-d'œuvre inter fonctionnel sur les projets de livraison.
- Diriger et soutenir l'approvisionnement du projet et la gestion des sous-traitants et fournisseurs tiers
- Participe aux différentes réunions des projets site (CAPEX, et aux autres Réunions liées à l’activité).
- Est force de proposition sur les actions de fiabilisation.
- Rédige le rapport et renseigne les documents nécessaires à l’activité.
- Participe à la formation des techniciens de maintenance.
- Participe à l’élaboration des plans de maintenance préventive et des gammes d’améliorations.
- Participe aux gammes opératoires des équipements.
- Participe à la préconisation des listes PDR des nouveaux équipements.
- Assurer l’installation et la mise en service de nouveaux équipements.
- Rédaction des URS pour l’acquisition des nouveaux équipements de procès.
- Participer et consultation des offres des nouveaux projets.
- Création déviation et change contrôle sur phénix et investigation.
- Considérations HSE pour la maintenance (permis, PTW, LOTO) Gestion des sous-traitants (sécurité, performance, coût) Coordination efficace entre la maintenance et l'exploitation du site Programmes d'étalonnage et de qualification périodique.
Qualifications requises du poste :
Compétences :
- Maîtriser le process industriel et les principales technologies des installations.
- Gestion des parties prenantes et des personnes – De manière transversale dans une organisation matricielle.
- Appliquer et faire respecter des prescriptions techniques et réglementaires.
- Elaborer et suivre des tableaux de bord, des plannings.
- Gestion de projet – Gestion de la sécurité, des budgets, des calendriers, des ressources et des risques pour des projets d'un montant maximum de 5 M€. Titre PMI PMP préféré.
- Ingénierie technique - Expérience en ingénierie des procédés de fabrication pharmaceutique. PE, P.Eng. Charter Eng. Désignation préférée
- Connaissances réglementaires - Familiarisation avec les BPF et les réglementations/normes de la FDA.
- Capacité d’analyser avec méthode et résoudre les problèmes d'ordre technique ou relationnel.
Formation / Expérience professionnelle nécessaire :
- BTS ou ingénieurs en Maintenance industrielle.
- 05 ans minium dans un poste similaire ou équivalent.
- Maitrise de la langue anglaise.
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