Description Siamo alla ricerca, per conto di un’importante azienda del settore biomedicale, di un Process Engineer. Responsabilità: Design and qualification of manufacturing processes (mechanical, electrical, software, IO data), revising components and external processes in a global DFM logic. Development, optimization, and upgrading of manufacturing processes, including test plan validation strategy, from inception to startup and certification, with periodic re-validation and evaluation strategies. Execution of validation strategies and preparation of technical documentation. Conducting Process Failure Mode and Effect Analysis (FMEA) from inception to startup, root cause analysis, and updates for continuous improvement. Review of change proposals, standardization, and implementation based on design transfer rules. Identification of continuous improvement opportunities within the plant to maintain and enhance process performance. Define requirements for new manufacturing equipment and tools, validating their intended use with an optimal balance of quality and cost. Day-to-day problem solving and CAPA processes. Requisiti richiesti: Minimum 5 years of experience in process or product industry technical teams. Master's degree in Mechanical, Biomedical, Industrial Production, Aerospace Engineering, or Mechatronic Technical Diploma. Intermediate level knowledge of process validation methodology. Intermediate manufacturing know-how. Basic prototyping technology skills. Intermediate critical approach. Intermediate self-time management. Proactive and concise communication skills. Intermediate proficiency with informatics tools. Intermediate English language skills. Green Belt Certification in statistical analysis and problem solving are pluses. Sede di lavoro: Provincia di Vercelli, al confine con Torino. Tipo di contratto: Contratto a tempo indeterminato, con inquadramento da definire in base a competenza ed esperienza. J-18808-Ljbffr