Staff Systems Verification Engineer: Digital Projects

Smith & Nephew

Hull, United Kingdom
Generous annual bonus; pension schemes; car allowa...
**
7+ years product development experience
Medical device regulatory compliance
Hardware and software integration testing
** Smith & Nephew is seeking a Staff Systems Verification Engineer to lead testing strategies for innovative digital products in their Advanced Wound Management division. The ideal candidate will have extensive experience in product development and medical device testing, particularly with electromechanical devices. **

Job Summary

  • The role involves leading system-level testing and validation strategies for innovative digital wound care products.
  • Candidates must ensure compliance with FDA, ISO 13485, and IEC 62304 standards while managing complex hardware-software systems.
  • Smith & Nephew offers a hybrid work model with generous benefits including pension schemes, health plans, and flexible vacation.

Matching Summary

Match Score: 75

** Smith & Nephew is seeking a Staff Systems Verification Engineer to lead testing strategies for innovative digital products in their Advanced Wound Management division. The ideal candidate will have extensive experience in product development and medical device testing, particularly with electromechanical devices. **

Salary

Generous annual bonus; Pension schemes; Car allowance included

Skills & Requirements

Must-have

  • 7+ years product development experience
  • Medical device regulatory compliance
  • Hardware and software integration testing
  • Test environment automation development
  • Wireless communication protocols (BLE, Zigbee)
  • ISO 13485 and IEC 62304 knowledge

Nice-to-have

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

Key Requirements

  • Bachelor's degree in Engineering or Computer Science
  • 7 years of experience in medical device development
  • Knowledge of FDA CFR Part 820 regulations
  • On-site availability in Hull required

Work Rights

Not specified

Tailored Resume

Cover Letter