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Job description
QuidelOrtho is seeking a Quality Lead, Requirements and Specifications Management (Assay) to own the end-to-end quality inputs for a portfolio of assay-based medical devices. You will partner with R&D, Systems Engineering, Regulatory Affairs, Manufacturing, and Product Management to ensure compliant, scalable, and high-quality product development.
The role requires a Bachelor’s degree in Life Sciences or Engineering and 7+ years in Quality/Compliance in the Medical Device/IVD sectors, with
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Who can apply
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