Job Description

Description

Siamo alla ricerca di un Process Engineer da inserire in importanti progetti in ambito biomedicale.

Responsabilità:

  • Responsible for design and qualification of manufacturing processes (mechanical/electrical/software/IO data), critically revising components and external processes in a global DFM logic

  • Responsible for development/optimization/upgrade of manufacturing processes, relative test plan validation strategy, from inception, identifying appropriate technology, through to startup and certification including periodical re-validation need strategy and need evaluation

  • Responsible for Validation strategy execution and tech documentation preparation

  • Responsible for manufacturing flow Process Failure Mode and Effect Analysis from inception to startup, root cause analysis and update in the frame of continuous improvement

  • Responsible for change proposal review and standardization and relative implementation based on design transfer rules

  • Responsible for Continuous Improvements identification within the plant aimed to maintain and improve processes performances

  • Responsible to define requirements for new manufacturing equipment and tool validating the intended use with the better compromise of quality/cost

  • Responsible for day by day problem solving and CAPA processes


    • Requisiti richiesti:

  • Minimum 5 years of experience in process or product industry's technical teams

  • Master degree in Mechanical, Biomedical, Industrial Production or Aerospace Engineering or Mechatronic Technical Diploma

  • Process validation methodology - Intermediate level

  • Manufacturing know how - Intermediate level as minimum

  • Prototyping technology - Basic level

  • Critical approach - Intermediate level

  • Self- time management - Intermediate level

  • Communication based on proactive and synthetic exchange

  • Use of informatics tool - Intermediate level as minimum

  • English language - Intermediate level as minimum

  • Statistical analysis approach - Green Belt Certification as plus

  • Problem solving methodology - Green Belt Certification as plus


    • Sede di lavoro:
    Sede di lavoro: provincia di Vercelli, al confine con Torino


    Tipo di contratto:
    - Contratto a tempo indeterminato, con inquadramento da definire in funzione di competenza ed esperienza acquisite
     

    Required Skills
    - esperienza nel ruolo
    - laurea in ingegneria biomedica o meccanica o industriale/gestionale
    - conoscenza processi in ambito manufacturing

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