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Industrialization Engineer

Buscojobs

Sardegna

In loco

EUR 40.000 - 55.000

Tempo pieno

5 giorni fa
Candidati tra i primi

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Descrizione del lavoro

A leading company in the medical device sector is seeking an experienced candidate for an industrialization role. The position involves transitioning products from development to production, optimizing processes, and ensuring compliance with regulatory standards. The ideal candidate will have a strong background in engineering and technical documentation, with a focus on collaboration and problem-solving.

Competenze

  • At least 3 years of experience in a similar role.
  • Ability to interpret electrical schematics and mechanical drawings.

Mansioni

  • Collaborate with R&D and manufacturing for product transition.
  • Optimize manufacturing processes and validate them.
  • Conduct risk assessments and analyze production issues.

Conoscenze

Collaboration
Problem Solving
Technical Documentation

Formazione

High school diploma
Bachelor’s degree in Industrial Engineering

Strumenti

Electrical Schematics
PCB Layouts
Mechanical Drawings

Descrizione del lavoro

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:

  • Collaborate closely with R&D and manufacturing teams to ensure a smooth transition from prototype to full-scale production.
  • Optimize wiring harnesses and integrate electronic modules into electromechanical systems.
  • Define and optimize manufacturing processes, introducing new technologies as needed.
  • Support the validation of manufacturing processes (IQ, OQ, PQ) in accordance with regulatory standards.
  • Lead prototype activities.
  • Prepare and update technical documentation (Work Instructions, prototype assembly reports, test protocols, test reports, etc.).
  • Conduct risk assessments of equipment and processes (PFMEA).
  • Perform root cause analysis of complaints and produce reports.
  • Analyze and resolve production issues to improve efficiency, quality, and cost.
  • Work closely with suppliers and production teams to optimize components and processes.
  • 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, shielding.
  • Proficiency in writing technical documentation (specifications and reports).
  • Ability to work independently and as part of a team.
Educational Requirements
  • High school diploma (scientific, mechanical, or similar) or bachelor’s degree in Industrial, Electronic, or Biomedical Engineering.
  • Proficiency in written and spoken English (level B1).

The compensation will be commensurate with experience.

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