About the role

Our Senior Software Engineer looking for an experienced embedded software engineer to help bring our latest products to life. This role is an opportunity for someone to architect, design and prototype software applications, real time software applications for use in various Smith and Nephew products, meet customer needs, manufacturability, cost, quality, reliability, effectiveness, usability. The post holder has responsibility for software / firmware engineering areas required to deliver a new product development and is required to work closely with Operations Personnel, Functional Managers and Senior Engineering and Technical personnel (site based and third party) to ensure effective delivery is achieved.

This process will require collaborative efforts from others inside and outside of R&D, who will help craft testing methods and ultimately products that are not just efficient to manufacture but commercially viable. More importantly, it should keep our customers firmly in centre of everything we do!
Sound good? Here are some of the expectations in the role:

Responsibilities:

Lead key software engineering work-stream activities in the establishment of new product development facility including supporting required quality system obtainment

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  Perform design control functions to ensure compliance with FDA, ISO, and other QSRs
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  Design and write the embedded software code according to desired specifications
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  Responsible for writing product specifications, design/test documents in addition to conducting technical design reviews as needed.
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  Perform Software risk analysis with internal cross functional team
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  Conduct hands-on technical leadership in the development of medical device software
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  Support software QA working instruction/template creation and improvement.
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  Provide post-production support
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  Assess third party and open-source software.

Work in collaboration with other highly skilled engineers to bringup new hardware, including the implementation of low level drivers and frameworks.
Create technical documentation as required by the team, ensuring that the project file is suitable for relevant notified bodies, and to present the project at such audits.

Minimum Requirements:

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  Bachelors degree in a relevant Engineering/Science subject area
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  At least 5 years\xe2\x80\x99 experience in a regulated industry with recent experience of product registration and launch.
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  Experience in Software / Firmware Engineering for medical device and working knowledge of design control.

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