Descrizione Siamo alla ricerca, per conto di un'importante azienda del settore biomedicale, di un Process Engineer.
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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