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DescripciónDescription
Coordinates and control preparation and/or changes of documentation such as engineering drawings, specifications, quality inspection criteria, standard operating procedures etc. Maintains control of documentation changes approval process and documentation master files. Responsible for processing documentation requests and distribution of controlled documents, watermark controlled forms and related Tracking Logs to the different areas. Processes and provides document requests for revision or reference , as applicable.
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Requisitos Requirements
Education and/or Experience: Associate Degree. A minimum of two- 2 years experience in a similar position in an FDA regulated environment preferred.
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