Manufacturing engineer
Vor 3 Tagen
Nous recherchons un/e Manufacturing engineer pour un de nos clients sur le canton de Neuchâtel.
Si vous souhaitez travailler dans une atmosphère agréable et dynamique dans le domaine des dispositifs médicaux ce poste est pour vous.
Il s’agit d’un contrat temporaire à durée illimitée.
Vos responsabilités:
- Participe aux cellules de production en tant que responsable Manufacturing engineering et supporte le business pour toute contribution technique clé.
- Fournit les données d’ingénierie pour résoudre des problèmes complexes de process de production, dans un environnement d’assemblage d’implants médicaux, en mettant en place des solutions efficaces financièrement et maîtrisées en termes de planning.
- Assure le suivi du support de production et sa présentation au niveau intermédiaire de management.
- Donne les données techniques nécessaires à l’établissement des phases de planification, de conception, de développement et de validation des processus de production.
- Dirige les investigations techniques et les études de faisabilité requises.
- Conçoit, développe et met en production des équipements et des outillages ; exécute les qualifications d’installation associées et les activités de validations.
- S’assure que toute activité est gérée dans le respect des normes applicables et procédures internes et externes,pour les aspects Hygiène, Sécurité et Environnement, Régulatoire (GMP, ISO; FDA, Procédures internes) et Système Qualité.
- Maintient conforme la documentation de support de production et suggère des améliorations pour les systèmes et les procédures.
- Applique une méthodologie de management de projet pour délivrer la mise en service des équipements et des produits.
Votre profil:
- Diplôme d’Ingénieur en mécanique / micromécanique / sciences des matériaux
- Jeune diplômé(e) accepté
- Maîtrise du français et niveau Intermediate / Upper intermediate en anglais
Qualifications Requises:
- Compétences techniques et méthodologies de l’ingénieur
- Maîtrise de la lecture et du tolérancement de plans.
- Bien organisé et tourné vers la production de résultats.
- Autonome, avec l’attention du détail.
- Aptitude à travailler en équipe cross-fonctionnelle (R&D, Quality Engineering, Procurement, Manufacturing, HSE).
- Bonnes capacités de communication, rendant facile à comprendre des problématiques complexes, aptitude à préparer des supports de communication pour un niveau de management intermédiaire.
- Maîtrise des outils Office et de tous les outils standards informatiques.
Qualifications souhaitées mais non requises:
- Connaissance des exigences de validation du Medical Device.
- Connaissance des méthodologies Process Excellence (Lean Manufacturing, Six Sigma).
- Connaissance des systèmes d’entreprise (ERP / PLM / Quality system).
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