Description
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
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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