Medical Device R&D Lead

Medacta Italia

Rancate

Vor Ort

CHF 110.000 - 150.000

Vollzeit

vor 41 Stunden
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Carpooling organized by Medacta
Public transport incentives
Continuous training
Annual salary review

Zusammenfassung

Medacta International in Switzerland is seeking a design and development engineer to lead the creation and refinement of medical devices and surgical instruments. You will drive CAD design, finite element analysis, verification/validation, and cross-functional execution from concept through transfer to manufacturing.

The role requires translating clinical needs into user-centered product requirements, collaborating with clinical advisors, and supporting regulatory documentation and IP activities

Qualifikationen

  • Master’s degree in Mechanical or Biomechanical Engineering.
  • CAD modeling with SolidWorks.
  • Strong project management and cross-functional coordination.
  • Working knowledge of regulatory pathways (FDA, CE, TGA).
  • Experience compiling Technical Files with V&V documentation.
  • Experience with manufacturing support and cost optimization.
  • Exposure to IP processes and patent analysis.
  • Ability to define mechanical test protocols and report results.
  • English required; Italian is a plus.

Aufgaben

  • Create and iterate 3D designs and drawings in SolidWorks with DFM/DFA.
  • Prepare clear written and oral communications for stakeholders.
  • Plan and manage projects across R&D, Quality, Regulatory, Manufacturing, and Marketing.
  • Execute and document Technical File activities including V&V.
  • Support manufacturing and suppliers to optimize process capability and cost.
  • Assist with patent searches and IP-related activities.
  • Define mechanical test protocols and report results.
  • Translate clinical needs into user-centered product requirements.
  • Interface with clinical advisors for input on design and evaluation.

Kenntnisse

SolidWorks design
Project management
DFM/DFM
Technical communication
Regulatory collaboration

Ausbildung

Master’s degree in Mechanical or Biomechanical Engineering

Tools

SolidWorks

Jobbeschreibung

Medacta International in Switzerland is seeking a design and development engineer to lead the creation and refinement of medical devices and surgical instruments. You will drive CAD design, finite element analysis, verification/validation, and cross-functional execution from concept through transfer to manufacturing.

The role requires translating clinical needs into user-centered product requirements, collaborating with clinical advisors, and supporting regulatory documentation and IP activities

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