Design Engineer I

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.

ESSENTIAL DUTIES AND RESPONSIBILITIES

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.

EDUCATION & EXPERIENCE REQUIREMENTS

Bachelor's degree in Mechanical or Biomedical Engineering or related field
Master's or Min 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
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.

Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.

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Accommodation Statement

If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to [email protected] with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.

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