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Design Engineer

Req ID: J2320749

  • Ubicación
    Bray, Dublín, Ireland
  • Categoría Grupo de Servicios de Diseño
  • Publicado miércoles, 8 de junio de 2022
  • Tipo Tiempo completo
  • Tipo de Empleo Empleado Permanente

Descripción del Trabajo



Responsible for the design, development and verification of complex medical and diagnostic devices with a major focus on injection moulded components.

Applies mechanical, manufacturing, and medical engineering knowledge to develop devices from requirements and specification to product introduction.

Participates in cross-organisational efforts to design, develop, and implement robust designs with appropriate verification, design for manufacturability and regulatory compliance for seamless product introduction.


  • Delivers design, development and verification of complex assemblies, sub-assemblies, components, and packaging as assigned.
  • Product design and CAD generation of complex medical device designs using SolidWorks. Generate design concepts, proposal, and presentation.
  • Participates in definition of product requirements into product specifications
  • Undertakes prototype manufacture and assembly
  • Participates in evaluation of product specifications through engineering study and proof of concept testing
  • Materials selection and review
  • Develops and implements changes to existing product to achieve performance, quality, and cost improvements
  • Contributes to product and manufacturing risk assessment / analysis documentation (PHA, FTA, dFMEA, uFMEA)
  • Analyses data and conducts failure investigations to determine causes of problems and develop & implement solutions
  • Applies structured approach to all deliverables involving key stakeholders with ability to communicate effectively both internally and externally.
  • Contribute to technical meetings and presentations both internally and with external customers
  • Research new technology or development tools to remain informed of current innovations.
  • May perform other duties and responsibilities as assigned.


  • Bachelor's degree in Mechanical or Biomedical Engineering or related field
  • Minimum of 1-3 years of related experience and/or training
  • Competency in CAD Modelling (Preferably Solidworks / Creo)
  • Understanding/Competence in Tolerance Analysis, 2D Drawings, GD & T, FEA analysis desirable
  • Knowledge of engineering theories, design principles and practices, and design evaluation techniques.
  • Knowledge and understanding of regulatory requirements for medical devices including ISO13485
  • Excellent problem-solving skills
  • Ability to work in a team environment
  • Strong analytical capabilities
  • Excellent attention to detail
  • Ability to work on own
  • Strong attention to detail and Quality focus.
  • Proven documentation writing skills; clear and concise using objective evidence and language.
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