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DOUGLAS PAUL ��C�'�' <br />2468 N�rt1� Iiar�.l�z�� Av�u� <br />Ros�ville, MN 55113 <br />Home (651) 697-9183 C�ll (651) 247-0335 <br />doroot@corncast.net <br />�iT14���RY <br />Ex��e�-ienced analytical ch���aist�y leade� with zzaarza�egi�ent experience u� Analytical Method <br />develo��nse��� and validation, Quality Control, Quality Assurance, and Product Development. <br />Successful zalanagcrraezat of cGMP compliance for APIs, exeipients, components, and drug <br />products. Leader of product development and production teams. Rapid, e�F'icient pxa�xams for <br />analytical method development, validation, and transfer for effective CMC docuz�e�ta�in�. <br />y'�i}i�.��rr�T�. <br />��LSTA`T' CORPORATION 2004 - Present <br />A start up OTC health care products company focussed on t�aetinen�s for migraine, sinus <br />congestion, and sleep products. <br />Chief Scientist <br />2004 - Present <br />Responsibilities - New product development �abor�tr�_r;r <br />- Technical support for existing product <br />- Cozrdinatia� of contract manufacturing <br />BOSTON SCIENTIFIC CORPORATION INC. 2003 - 2004 <br />A world-wide leader in medical devices for mi�irnally invasive surgery. Over 14,000 <br />products and 15,000 employees with headquarters in Natick, ���f;'�. <br />Manager Operations Analytical Laboratory 2003 -� 2004 <br />Responsibilities - Management of laboratory staff <br />- Release testing for `� �us 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 />A� entrepr��eur�ial drug delivery company focused o�. orally disintegrating tablets. OTC and <br />prescription products in several therapeutic areas developed ��;h support fronl large <br />pharmaceutical partners. Res�onsi�i�ities completed in October 2002 <br />Director, Quality Ass�ra�ac� 2001 - 2002 <br />Responsibilities - Management of Quality Assurance staff <br />- Review and Approval o�all Validation Doc��neiits <br />, Dev�Iopment of Product Speciiication for new products <br />- Controlled dacu�nent revision, distribution. a��d control <br />T Production line audits and corrective actions <br />- Incoming n�afe�ial receipt, sampling, testing and disposition <br />Selected T Ti �,-:-i ��:�� � - New efficient system for doc�u�l��lf revision n�,rF con*�-o1 <br />F Ne�� hatch records for efficient production and review <br />•- Hosted successful Iv�C� 1're-f���proval Inspection <br />