Medical Device Quality Engineer | ISO 13485 & FDA QSR
Job in
Gloucester, Gloucestershire, GL1, England, UK
Listed on 2026-07-21
Listing for:
Omega Resource Group
Full Time
position Listed on 2026-07-21
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
Omega Resource Group seeks a Quality Professional – Day Shift in Gloucestershire to ensure medical devices meet ISO 13485, FDA 21 CFR Part 820, and MDR/IVDR requirements across design, manufacture and release.
You will own the QMS, lead CAPA and non-conformance investigations, drive IQ/OQ/PQ validation, and support risk management per ISO 14971 while collaborating with R&D, Manufacturing and Regulatory teams.
#J-18808-LjbffrNote that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
Search for further Jobs Here:
×