Process Engineer

Albelissa Engineering, IT & Digital Solutions · Chivasso, Piemonte, Italia · · 50€ - 70€


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  • 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
  • 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
  • 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
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

Seniority level

  • Seniority level

    Mid-Senior level

Employment type

  • Employment type

    Part-time

Job function

  • Job function

    Management and Manufacturing

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