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BioPharma Technical Writer /QC Associate resume in Stroudsburg, PA - March 2014
SUMMARY:
A Validation Engineering Technical Writer who performs Best Practices QA
Commissioning Document Review and Revision. Project Change Control
documentation DCO tracking, cGMP practices, Research and Development, FDA
Part 11, 210 &211 and 820 requirements for GMP's, GDP's, Document...
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