Lead QA Engineer – Medical Device Embedded Software Testing

Lead QA Engineer – Medical Device Embedded Software Testing

Contract Type:

Contractor

Location:

Motherwell

Industry:

IT

Contact Name:

James Dryden

Contact Phone:

+44 (0)20 7002 0057

Date Published:

22-Sep-2026

Lead QA Engineer – Medical Device Embedded Software Testing

Up to £660/day | Inside IR35 | Hybrid – Motherwell, Scotland

Previous hands-on experience testing embedded software within medical devices is essential. We can only consider candidates who meet this requirement.


This is a specialist device-software testing contract. General web/application QA, pharmaceutical Computer Systems Validation (CSV), manufacturing validation or quality management experience alone will not meet the brief.

You’ll lead and execute software testing for a standalone medical device used for diagnostics and patient monitoring, delivering V&V evidence for an FDA 510(k) submission and a subsequent commercial software release.

Location flexibility

Applications are welcome from local candidates and those based further away who can travel to Motherwell:

  • Within an hour of Motherwell: 2 days per week onsite.
  • Further away: 2–3 days per month onsite may be agreed for the right candidate.

Contract details

  • Rate: Up to £663/day, Inside IR35
  • Start: 1 October
  • Duration: 3 months initially, with a further period of at least 12 months anticipated

What you’ll do

  • Write and execute test cases against embedded medical-device software.
  • Produce documented verification and validation evidence.
  • Report, investigate and manage software defects through to resolution.
  • Contribute to impact analysis, risk analysis and FMEAs.
  • Manage testing priorities using Jira sprint boards.
  • Support regulatory submission and commercial release deadlines.

Essential experience

  • Personally writing and executing tests for software embedded within a medical device.
  • Medical-device software V&V within a regulated development environment.
  • Documenting test results and linking evidence to requirements.
  • Risk-based testing and contribution to risk-management activities.
  • Leading testing activities while remaining hands-on.

Experience supporting an FDA 510(k) submission is highly desirable.




To apply, send your CV, availability, location and day-rate expectations. Please name the medical device(s) you’ve worked on and briefly describe the embedded software testing you personally performed.

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