Industrialization Engineer

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

Descrizione del lavoro

An established industry player in medical devices is seeking a skilled industrialization engineer to lead the transition of products from development to large-scale production. This role involves close collaboration with R&D and manufacturing teams to optimize processes, conduct risk assessments, and prepare technical documentation. The ideal candidate will have a strong background in regulated industries, with hands-on experience in wiring design and a knack for problem-solving. Join a dynamic team where your contributions will drive innovation and enhance product quality.

Competenze

• 3+ years of experience in a similar role, especially in regulated industries.
• Hands-on experience with wiring design and optimization.

Mansioni

• Collaborate with R&D and manufacturing for product transition.
• Define and optimize manufacturing processes and technologies.
• Monitor production KPIs for continuous improvement.

Conoscenze

Interpretation of electrical schematics

Wiring design and optimization

Technical documentation writing

Root cause analysis

Risk assessment (PFMEA)

Formazione

High school diploma in scientific or mechanical fields

Bachelor’s degree in Industrial, Electronic, or Biomedical 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 successful candidate will perform industrialization activities for new and revised products. The resource is responsible for transitioning products from development to large-scale production.

Essential Duties and Responsibilities

The candidate, supervised by the Industrialization Manager, will perform the following activities:

1. Collaborate closely with R&D and manufacturing teams to ensure a smooth transition from prototype to full-scale production.
2. Optimize wiring harnesses and integrate electronic modules into electromechanical systems.
3. Define and optimize manufacturing processes, introducing new technologies when needed.
4. Support the validation of manufacturing processes (IQ, OQ, PQ) in accordance with regulatory standards.
5. Lead prototype activities.
6. Prepare and update technical documentation (Work Instructions, prototype assembly reports, test protocols, test reports, etc.).
7. Conduct risk assessments of equipment and processes (PFMEA).
8. Perform root cause analysis of complaints and produce reports on findings.
9. Analyze and resolve production issues to improve efficiency, quality, and cost-effectiveness.
10. Work closely with suppliers and production teams to optimize components and processes.
11. Monitor production KPIs and propose 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 (e.g., automotive, 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.

Experience 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.