Senior Quality Control Project Manager

vor 1 Tag


Genf, Schweiz Teoxane SA Vollzeit

Acteur majeur indépendant de la médecine esthétique et de la dermocosmétique, les Laboratoires Teoxane se consacrent aux hommes et aux femmes qui souhaitent se sentir au mieux d'eux-mêmes tout au long du temps, en repoussant les limites de la médecine esthétique et en challengeant le marché. Ainsi nous inventons des solutions sûres, prouvées, inspirées par les milliers de patients que les cliniciens rencontrent chaque semaine. Notre maîtrise de l'acide hyaluronique nous permet de proposer des produits de comblements et des dermocosmétiques de la plus haute performance, dans plus de 90 pays dans le monde et d'être le 3ème acteur mondial des fillers à base d'acide hyaluronique.

Dans le cadre de notre fort développement, nous recrutons un/une :

Senior Quality Control Project Manager

Activités principales

  • Être Project Manager Qualité des projets d'amélioration stratégiques du Contrôle qualité permettant l'amélioration et la business continuity tout en garantissant la conformité avec le Système de Management de la qualité (SMQ) :
    • Recueillir les besoins (Mind map, Project Charter -),
    • Être responsable des changes control en lien avec les projets
    • Rédiger la documentation Qualité des projets tel que le Plan Qualité Projet (PQP)
    • Rédiger la documentation liée aux projets (Procédures, instructions, formulaires-
  • Être équipier CQ dans le cadre des projets d'intégration de nouveaux produits et de nouvelles méthodes :
    • Rédiger les besoins du service contrôle qualité et autres documents associés,
    • Suivre et accompagner les activités de Design Transfer Analytique,
    • Rédiger des procédures, instructions et autres documents qualités en lien avec les projets,
    • Participer aux meetings projets de travail et de pilotage,
  • Gérer les interventions fournisseurs et/ou les envois des équipements pour maintenance préventive/Curative
  • Conduire les initiatives d'amélioration continue au sein du laboratoire CQ
  • Animer les routines d'amélioration continue du laboratoire CQ
  • Effectuer toute autre mission particulière qui pourrait vous être confiée par la Direction

Votre profil

  • Bachelor Universitaire, EPF ou HES, diplôme de technicien ES ou formation jugée équivalente
  • 10 ans d'expérience dans le secteur pharmaceutique ou du dispositif médical
  • Expertise HPLC/UPLC
  • Orientation résultat, capacité à prendre des décisions et à communiquer
  • Anglais niveau B1 minimum

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