Global Quality Lead: Assay & Specs
Listed on 2026-10-26
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Quidel Ortho in the United Kingdom seeks a Quality Lead, Requirements and Specifications Management (Assay) to drive end-to-end quality for assay-based medical devices. You will own the design inputs, enable compliant, scalable product development, and partner with R&D, Regulatory Affairs, Manufacturing, and Product Management.
The role requires 7+ years in Quality/Compliance within medical devices, ISO 13485 and FDA/IVDR knowledge, and a proven ability to lead cross-functional initiatives.
Consider building your career as a Global Quality Lead:
Assay Requirements & Specs at Ortho Clinical Diagnostics.
All applications are reviewed carefully by our team.
The position is based in Bridgend, Wales, United Kingdom.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 101..
We aim to respond to suitable candidates as soon as possible.
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