Smith+Nephew
Medical Technology
SeniorR&DEngineer
Neural analysis suggests this role is
optimal for Senior candidates.
“Senior R&D Engineer at Smith+Nephew. Skills: medical device design, product development, design control, verification and validation. Lead design, development, verification, validation. Define user needs”
What You'll Achieve.
improve patients’ lives worldwide
Industry & Context.
What They're Looking For.
Must Have
Bachelor of Science in Engineering, minimum of 4 years of relevant experience, Master’s degree with at least 2 years of experience, PhD in Engineering or Science, experience with 3D CAD software, medical device design controls, CFR 820, ISO 13485, ISO 14971, Solid understanding of product development within a regulated environment, Ability to work independently, leading technical activities within cross functional teams
Nice to Have
FEA, GD&T, statistical analysis, human factors engineering, usability assessments
What You'll Do.
Create product specifications
Develop verification and validation strategies
Provide technical input
How You'll Work.
Team & Collaboration
collaborate across global teams; key contributor and technical leader within cross functional project teams; stakeholder engagement; work independently while leading technical activities within cross functional teams
Full Job Description
**Life Unlimited.** At Smith+Nephew we design and manufacture technology that takes the limits off living. As a **Senior R &D Engineer**, you will play a key role in bringing innovative medical technologies from concept through launch. Based in **Memphis, Tennessee** , this is an opportunity to lead complex design activities, collaborate across global teams and directly impact products that improve patients’ lives worldwide. **What will you be doing?** * Leading the design, development, verification and validation of new medical devices from concept through design transfer and product launch * Serving as a key contributor and technical leader within cross functional project teams including marketing, manufacturing, quality and regulatory partners * Defining user needs and design inputs through literature reviews, stakeholder engagement and observational research * Creating and maintaining product specifications, 3D CAD models and associated technical documentation in line with design control and regulatory requirements * Developing and executing verification and validation strategies, including custom test methodologies where standards do not exist * Providing technical input to intellectual property activities, regulatory submissions and customer-facing materials * Mentoring and supporting the development of less experienced engineers **What will you need to be successful?** * Bachelor of Science in Engineering with a minimum of 4 years of relevant experience, or a Master’s degree with at least 2 years of experience, or a PhD in Engineering or Science * Strong experience with 3D CAD software and medical device design controls including CFR 820, ISO 13485 and ISO 14971 * Solid understanding of product development within a regulated environment * Ability to work independently while leading technical activities within cross functional teams * Experience or exposure to FEA, GD&T, statistical analysis, human factors engineering or usability assessments is preferred **Yo
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