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See the original post from: Novo Nordisk
Summary:
Position Purpose: Primary responsibility is to provide quality review & approval of validation activities associated with changes to existing systems & projects that support site Clayton. Support protocol development & approval, investigations for deviations & champion local, corporate & regulatory standards. Presentation & support for validation concepts & approaches with audits & inspections. Provide Quality validation review & approval through the preparation, execution, data analysis, & report writing for IQ, OQ & PQ protocols. Quality review & approval of Change Requests (CR?s) ...
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