Staff Systems Verification Engineer: Digital Projects

Smith+Nephew

Hull, United Kingdom
Generous annual bonus; pension schemes; save as yo...
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7+ years product development experience
Medical device regulatory compliance
Hardware and software integration testing
** Smith+Nephew is seeking a Staff Systems Verification Engineer to join their Advanced Wound Management division in Hull, UK. The role focuses on developing and executing test strategies for digital and electromechanical medical devices, requiring extensive experience in product development and compliance with industry standards. **

Job Summary

  • The role involves leading test strategies for innovative digital wound care products combining hardware and software.
  • Candidates must ensure all testing activities comply with FDA, ISO 13485, IEC 62304, and MDR design control requirements.
  • Smith+Nephew offers a hybrid working model with flexible vacation, generous bonuses, and comprehensive health benefits.

Matching Summary

Match Score: 75

** Smith+Nephew is seeking a Staff Systems Verification Engineer to join their Advanced Wound Management division in Hull, UK. The role focuses on developing and executing test strategies for digital and electromechanical medical devices, requiring extensive experience in product development and compliance with industry standards. **

Salary

Generous annual bonus; Pension schemes; Save As You Earn share options; Car allowance

Skills & Requirements

Must-have

  • 7+ years product development experience
  • Medical device regulatory compliance
  • Hardware and software integration testing
  • Test strategy and automation framework development
  • Wireless communication protocols (BLE, Zigbee, NFC)

Nice-to-have

  • Python, MATLAB, or LabVIEW proficiency
  • Master's or PhD in engineering field
  • Experience with Jama or DOORS requirement tools
  • Cross-functional collaboration skills
  • Remote team leadership experience

Key Requirements

  • Bachelor's degree in Engineering or Computer Science
  • 7 years experience in medical device product development
  • Knowledge of FDA 21 CFR Part 820 and ISO 13485:2016
  • Experience with IEC 62304 compliant software delivery
  • Ability to work on-site in Hull, UK

Work Rights

Not specified

Tailored Resume

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