Senior Design Engineer
5 days ago
We are seeking a highly skilled Senior Design Engineer to join our team at Jabil. The ideal candidate will have a strong background in mechanical engineering and experience with design for manufacturability and regulatory compliance.
The Senior Design Engineer will be responsible for the design, development, and verification of complex medical devices with a major focus on injection moulded components. This includes applying mechanical, manufacturing, and medical engineering knowledge to develop devices from requirements and specifications to product introduction.
The successful candidate will participate in cross-organisational efforts to design, develop, and implement robust designs with appropriate verification, design for manufacturability, and regulatory compliance for seamless product introduction.
- Main Responsibilities:
- Deliver design, development, and verification of complex assemblies, sub-assemblies, components, and packaging as assigned.
- Develop product design and CAD generation of complex medical device designs using SolidWorks.
- Generate design concepts, proposals, and presentations.
- Participate in definition of product requirements into product specifications.
- Undertake prototype manufacture and assembly.
- Contribute to product and manufacturing risk assessment/analysis documentation (PHA, FTA, dFMEA, uFMEA).
- Analyse data and conduct failure investigations to determine causes of problems and develop solutions.
- Apply 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.
Requirements:
- Bachelor's degree in Mechanical or Biomedical Engineering or related field.
- Master's or 1 year relevant experience preferred.
- Competency in CAD Modelling (preferably Solidworks/Creo).
- Understanding/competence in 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.
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