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and GMDN codes. Design, develop, test, document & support of cGxP systems as per 21CFR Part11 & US FDA. Responsible for qualification & validation (IQ/OQ/PQ), master plans, protocols, changes requests, gap & root cause analysis, risk management plans, traceability matrix,... 2025-06-02 22:35:37 – Posted by: jobvertise.com |
EDISON
NJ |