Project Engineer

Il y a 2 mois


Strasbourg, France PolyPeptide Temps plein

PolyPeptide Laboratories France à Strasbourg est la filiale française d’un Groupe international d’environ 1 100 personnes, leader mondial dans la recherche, le développement et la production de peptides de synthèse. Société prestataire de service pour l’Industrie Pharmaceutique, PolyPeptide Laboratories France considère que l’innovation et la technologie sont les fondations de l’entreprise pour se positionner sur le marché et construire l’avenir.

Nous recherchons pour notre site de Strasbourg, dans le cadre d’un Contrat à Durée Indéterminée :

Un(e) Project Engineer

Rattaché(e) au Directeur Services Techniques, vous accompagner les managers dans la définition des besoins d’investissements et des choix techniques. Vous assurez également la réalisation des projets d’investissements et d’amélioration.

Vos principales missions

Ingénierie et travaux neuf

  • Réalisation des analyses des besoins auprès des clients internes et/ou externes
  • Rédaction de cahiers des charges en collaboration avec les utilisateurs finaux
  • Préparation des dossiers d’appel d’offres et suivi de la procédure d’achat
  • Préparation des dossiers techniques des nouvelles installations et suivi de leur mise à jour
  • Gestion des délais, des coûts des travaux neufs et investissements attribués
  • Mise en place et suivi du plan de prévention pour les interventions d’ingénierie relevant de sa responsabilité
  • Suivi de la réalisation des chantiers dans le respect des règles HQSE
  • Suivi des sous-traitants et coordination de leur activité sur le site

Qualité et documentation

  • Gestion et suivi des dossiers techniques des installations
  • Suivi de la traçabilité des modifications apportées sur les équipements
  • Participation à l’élaboration des protocoles de qualifications initiales

Profil recherché

  • Bac+5 - Ecole d’ingénieur généraliste
  • Une expérience probante dans les procédés chimiques et pharmaceutiques est souhaitée
  • Connaissances sur la validation des systèmes informatisés en environnement pharmaceutique (norme 21 CFR part 11)
  • Maîtrise de l’anglais

Qualités attendues

  • Capacité d'analyse et de synthèse
  • Aisance relationnelle
  • Rigueur, organisation et sens des priorités

Poste à pourvoir de suite.


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