Process Engineer

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:

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