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DOUGLAS PAUL ROOT <br />2468 i•Tart�..i�Ta,rni�e Avenue <br />Ros�ville, MN SS I 13 <br />Home (651) �9l-al�� �e11(651) 247-0335 <br />��ruotfrr�co����ast_i�et <br />s��i?���►��r <br />Experienced pharmaceutical scientist with leadership experience in analytical chemistry, quality <br />control, and quality assurance. Successful management of new product development and <br />regulatory compliance for prescription �n� over-the-counter(OTC) pharmaceuticals. <br />EXPERIENCE <br />GE�,�STAT CORPORATION <br />2004 - Present <br />A start up OTC health care products company focussed on treatments for migraine, sinus <br />congestion, and sleep disorders. <br />Chief Scientist <br />2004 - Present <br />�e�p�rz�ibzlit�es -1���� product deveiopment iaboratory <br />- Technical support for existing products <br />- Corrdimation of contract manufacturing <br />BOSTON SC�NTTFIC CORPORATION INC. 2003 - 2004 <br />A world-wide leader in medical devices for �i���� izz�aszve surgery. Over 14,000 <br />products and 15,000 employees with headquarters m Naticl�, MA. <br />Manager Operations Analytical Laboratory 2003 — 2004 <br />Responsibilities - Management of laboratory staff <br />Product release testing for .� a�us dr�,zg �I�ta�g 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 erzt�'epre�eurzal drug delivery company focused on �r��ly disintegrating tablets. OTC <br />and prescription products in several therapeutic areas developed with support from large <br />pharmaceutical partners <br />Director, Qualify Assurance 2001 - 2002 <br />�esponsi�ili�:ies - Management of Quality Assurance �tai�` <br />- Review and Approval of all ValidationDocuments <br />- Development of Product Specification for new products <br />- Controlled document revision, distribution, and control <br />- Production Iine audits and corrective actions <br />- Incoming material receipt, sampling, testing and disposition <br />Selected �i�i�l�ts -���� e�cient system for document revision and control <br />- New batch records for efficient production and review <br />- kaas�ep. succes��i ��.�i Fi. Pre-Approval Inspection <br />