QuidelOrtho 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.
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Contact Details:
Ortho Clinical Diagnostics Recruitment Team
