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DOUGLAS PAUL ROOT <br />2468 North Hamli�e Avenue <br />Roseville, �N 55113 <br />Home (fi51) 697-9IS3 Cell (651) 247-0335 <br />doroot@,comcast.net <br />. lu _i�_�' <br />Experienced, proven leader with management experience in Product Development, Quality <br />Control, and Quality Assurance. Successful management of US and internationalcGMP <br />compliance. Leader of product development and production teams. Rapid, efficient programs to <br />support product development and commercial manufacture. Clean, decisive product support for <br />rapid market launch and comprehensible regulatory compliance strategies. <br />�.► _ N , <br />G��STA'� CORPORATION 2004 - Present <br />A start up OTC health care products company focused on traetrnenis for migraine, sinus <br />congestion, and sleep products. <br />Chief Scientist <br />2004 - Present <br />Responsibilities - New product development laboratory <br />- Technical support for existing product <br />- Corrdination of contract manufacturing <br />BOSTON SCIENTIFIC CORPORATION iNC. 2003 - 2004 <br />A world-wide leader in medical devices for minimally irzvasive surgery. Over 14,000 <br />products and 15,000 employees with headquarters in Natick, MA. <br />Manager Operations Analytical Laboratory 2003 — 2004 <br />Responsibilities - Management of laboratory staff <br />- Release testing for Taa��s drug eluting stent <br />- Management of testing of in-process materials <br />- Management of component testing <br />CIMA LABS INC., Eden Prairie, MN <br />1999 - 2002 <br />An entrepreneurial drug delivery company focused on orally disintegrating tablets. OTC and <br />prescriptior� products in several therapeutic areas developed with support from large <br />p�a�ace�tical partners. Responsibilities completed in October 2002 <br />Director, Quality Assurance 2001- 2002 <br />Responsibilities - Management of Quality Assurance staff <br />- Review and Approval of all Validation Documents <br />- Development of Product Specification for new products <br />- Controlled document revision. distribution. and control <br />- Production line audits and corrective actions <br />- Incoming material receipt, sampling, testing and disposition <br />Selected Highlights - New efficient system for document revision and control <br />- New batch records for efficient production and review <br />� Hosted successful MCA Pre-Approval Inspection <br />