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Mechanical Engineer

Black Diamond Networks

Torino

Ibrido

EUR 40.000 - 60.000

Tempo pieno

Ieri
Candidati tra i primi

Descrizione del lavoro

A leading technology company is seeking an experienced R&D Mechanical Engineer to support programs focusing on active implantable device design and development. The role involves working on mechanical components and collaborating closely with various stakeholders. Candidates should have a degree in Mechanical or Biomedical Engineering, fluent Italian language skills, and at least 5 years of relevant experience. Hybrid work model available with occasional remote work.

Competenze

  • At least 5 years of experience in mechanical development and industrial production, preferably in medical projects/products.
  • Fluent in Italian and able to work on-site.

Mansioni

  • Drive technical exchanges supported by design tools with suppliers and internal stakeholders.
  • Build, monitor, and maintain project plans, budgets, and action plans.
  • Support the creation of Device Master Record documents in collaboration with Operations.
  • Lead the design transfer process and provide training during product ramp-up.
  • Implement continuous improvement strategies to optimize cost and performance.

Conoscenze

Mechanical development
Design and validation (CAD)
Fluent in Italian

Formazione

Degree in Mechanical Engineering, Biomedical Engineering, or related field

Descrizione del lavoro

Title :

R&D Mechanical Engineer (Implantable Devices)

Location :

Greater Turin, IT area (1 day remote)

Start Date :

July / September target start

Duration :

12 months (with option to convert to perm)

Description :

The client is seeking an experienced R&D / Mechanical Engineer to support R&D programs focused on active implantable device design, development, and manufacturing. The candidate will primarily work on the mechanical components of new products and R&D projects.

  • Drive technical exchanges supported by design tools (CAD, simulation, statistical analysis) with suppliers and internal stakeholders to draw pragmatic conclusions.
  • Build, monitor, and maintain project plans, budgets, and action plans within the area of responsibility.
  • Execute development processes for new products and modifications of existing ones, collaborating with internal and external stakeholders.
  • Create comprehensive Design History Files for the area of responsibility.
  • Support the creation of Device Master Record documents in collaboration with Operations.
  • Work with Operations to design manufacturing processes and tools.
  • Support manufacturing of prototypes and plan/risk mitigation activities accordingly.
  • Provide technical expertise and assistance to Production, including sourcing, component/product disposition, and change management.
  • Lead the design transfer process and provide training during product ramp-up and market phases as needed.
  • Design mechanical components and sub-assemblies.
  • Define and execute qualification plans for products and components.
  • Lead development of components and sub-assemblies with suppliers.
  • Participate in risk management planning and prepare technical files for regulatory submissions.
  • Promote reverse engineering, feasibility studies, patent research, and standard monitoring within the team.
  • Implement continuous improvement strategies to optimize cost, manufacturability, performance, and reliability of products.

Qualifications :

  • Degree in Mechanical Engineering, Biomedical Engineering, or related field.
  • Fluent in Italian and able to work on-site.
  • At least 5 years of experience in mechanical development, including design, validation (CAD and technical documentation), and industrial production, preferably in medical projects/products.
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