Senior Quality Engineer – MedTech, ISO Expert
Listed on 2026-10-13
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Engineering
Quality Engineering, Process Engineer, Regulatory Compliance Specialist
Arevna Limited in the Midlands is seeking a Senior Quality Engineer to drive quality across the full lifecycle of medical devices. You will champion ISO 13485, EU MDR/UK MDR compliance, and regulatory alignment while collaborating with R&D, manufacturing, and regulatory teams.
You will lead CAPA and NCR investigations, manage QMS changes, and oversee supplier quality and process validation to ensure compliant product releases and continuous improvement.
This is an excellent opening to take on the Senior Quality Engineer – Med Tech, ISO 13485 Expert role at Arevna Limited.
This role, Senior Quality Engineer – Med Tech, ISO 13485 Expert at Arevna Limited, could be your next career step.
Are you ready to take on the Senior Quality Engineer – Med Tech, ISO 13485 Expert role at Arevna Limited?
We would love to welcome a new Senior Quality Engineer – Med Tech, ISO 13485 Expert to our group in West Midlands, England, United Kingdom.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).