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Location: Boulder, Colorado -Please note this position is located in Boulder, Colorado- QUALITY ASSURANCE SPECIALIST I and II Responsible for quality oversight of incoming raw materials, manufacturing floor operations, facility qualification and routine support, and QC laboratory9/24/2014 Boulder, CO Save This Job
SUMMARY: The document control specialist is responsible for maintaining development, manufacturing and clinical trial material supply document related to development and commercial drug product projects. The responsibilities include interacting with contract manufacturing10/17/2014 Redwood City, CA Save This Job