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QA Regulatory Affairs Specialist - Medical Devices QA / Regulatory Affairs Specialist Description Job Summary: This QA/RA Specialist is responsible for maintaining and ensuring that the company quality system meets FDA requirements for class I medical devices (IVD and ASR). The QA/RA Specialist is also responsible for ensuring that products and their labeling meet all regulatory requirements (national and international). Essential Functions: - Manage and establish / maintain compliance with FDA QSRs (GMP) (including company registration, new. After registering you may be able to apply for this job directly (if still active) on ((None))'s site. Future job matches may be sent from Geebo approved job partners.
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