Smith+Nephew

Medical Devices

StaffSystemsVerificationEngineer:DigitalProjects

United Kingdom FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Staff candidates.

The Brief

“Staff Systems Verification Engineer: Digital Projects at Smith+Nephew. Skills: Systems Verification, Test Strategy, Test Automation, Medical Devices. Generate and implement system level testing. Develop and validate test environments”

Industry & Context.

Medical Devices
Eligibility Requirements

Up to 15% travel

What They're Looking For.

Must Have

Bachelor’s degree in Electrical Engineering, Computer Engineering, Software Engineering, Computer Science, a relevant scientific or engineering area, or sufficient relevant technical experience, At least 7 years’ experience in product development, Experience developing medical devices, Experience working on products that combine hardware and software, Experience delivering medical device software that complies with IEC 62304, Ability to work on-site in Hull with a team of engineers

Nice to Have

Master’s or PhD in Electrical Engineering, Computer Engineering, Software Engineering, Computer Science, a relevant scientific or engineering area, Experience with Python, Experience with MATLAB, Experience with LabVIEW

What You'll Do.

Generate and implement system level testing

Develop and validate test environments

and develop framework for integration testing

Create automated and manual environments

Perform test activities

Identify opportunities to improve team productivity

Provide test forecasts

Identify test lab needs

How You'll Work.

Team & Collaboration

Interact with system engineers, hardware designers and software developers; Act as a senior member in a team of system test engineers; Work effectively cross-functionally with Clinical, Design & Usability, Marketing, R&D, Quality, and Regulatory; Collaboratively define and execute initiatives

Communication Scope

Effectively communicate complex technical information to a non-technical audience

Process & Methodology

Test strategy and planning across the full product development lifecycle

Full Job Description

**Life Unlimited.** At Smith+Nephew we design and manufacture technology that takes the limits off living**.** Smith + Nephew’s Advanced Wound Management (AWM) division is on a journey to design and develop new innovative digital products that shape and redefine what is possible in wound care. We are looking for a passionate and experienced Engineer to join our Systems Testing Team The **Staff Systems Test Engineer** will act as a test lead on digital and electromechanical device projects, providing test strategy and planning across the full product development lifecycle. The successful candidate will bring a demonstrated track record and experience in developing and executing test strategies, including test automation tools and frameworks. The role will report to the AWM R&D Systems Test Manager. **What will you be doing?** * Responsible for generating & implementing system level testing and verification & validation strategy, including planning * Developing and validating test environments for testing battery operated low power microcontroller products, some with wireless PAN and LPWAN communications e.g. BLE, Zigbee, NFC, UWB, NB-IoT, LTE-M * Identifying the need for, evaluating, selecting, and developing the framework for medical device integration testing which includes creating automated and manual environments * Interacting with system engineers, hardware designers and software developers to develop and maintain an expert understanding of the systems * Acting as a senior member in a team of system test engineers in test efforts with internal and external resources, possibly in remote locations * Work effectively cross-functionally with Clinical, Design & Usability, Marketing, R&D, Quality, and Regulatory and others to ensure inputs are considered and accounted for in test execution * Performing test activities while ensuring compliance with quality policies, procedures, and practices including ISO 13485, IEC 62304, FDA and MDR design control requirements for

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