Industrialization Engineer

JR Italy; Genova; In loco; EUR 35.000 - 55.000; Tempo pieno

Descrizione del lavoro

An innovative company is seeking a skilled industrialization engineer to facilitate the transition of medical devices from development to production. This role involves collaborating with R&D and manufacturing teams, optimizing processes, and ensuring compliance with regulatory standards. The ideal candidate will have a strong background in manufacturing processes and the ability to analyze and resolve production issues. Join a forward-thinking team dedicated to advancing medical technology and improving patient outcomes in a dynamic and challenging environment.

Competenze

• 3+ years of experience in industrialization within regulated sectors.
• Ability to interpret electrical schematics and mechanical drawings.

Mansioni

• Collaborate with R&D and manufacturing for product transitions.
• Optimize wiring harnesses and integrate electronic modules.

Conoscenze

Wiring Design

Technical Documentation

Root Cause Analysis

Risk Assessment (PFMEA)

Manufacturing Process Optimization

Formazione

High School Diploma

Bachelor's Degree in Industrial Engineering

Descrizione del lavoro

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Mectron spa, a company that designs and produces medical devices, is looking for a qualified candidate.

Position Summary

Reporting to the Industrialization Manager, the selected candidate will perform industrialization activities for new and revised products. The role involves transitioning products from development to large-scale production.

Essential Duties and Responsibilities

The candidate, supervised by the Industrialization Manager, will be responsible for:

• Collaborating closely with R&D and manufacturing teams to ensure a smooth transition from prototype to full-scale production.
• Optimizing wiring harnesses and integrating electronic modules into electromechanical systems.
• Defining and optimizing manufacturing processes, including introducing new technologies when necessary.
• Supporting the validation of manufacturing processes (IQ, OQ, PQ) in compliance with regulatory standards.
• Leading prototype activities.
• Preparing and updating technical documentation such as Work Instructions, prototype assembly reports, test protocols, and test reports.
• Conducting risk assessments of equipment and processes (PFMEA).
• Performing root cause analysis of complaints and generating reports.
• Analyzing and resolving production issues to enhance efficiency, quality, and cost-effectiveness.
• Working closely with suppliers and production teams to optimize components and processes.
• Monitoring production KPIs and proposing solutions for continuous improvement.

Work Experience – Required Qualifications

At least 3 years of experience in a similar role, preferably within the medical device industry or other highly regulated sectors such as automotive or aerospace.

Ability to interpret electrical schematics, PCB layouts, and mechanical drawings.

Knowledge of raw material transformation processes (metal machining, forming, injection molding).

Hands-on experience with wiring design and optimization, including harnesses, connectors, and shielding.

Proficiency in writing technical documentation (specifications and reports).

Ability to work independently and as part of a team.

Educational Requirements

High school diploma (preferably in scientific, mechanical, or similar fields) or a bachelor’s degree in Industrial, Electronic, or Biomedical Engineering.

Proficiency in written and spoken English (level B1).

The compensation will be commensurate with experience.