Timpel Medical
Christie Rose has a diverse and extensive work experience. Christie is currently working at Timpel Medical as the VP of Sales & Marketing since February 2020. Prior to this, they held the position of VP of Sales & Marketing at Respiratory Motion, Inc. from January 2018 to December 2019. Christie also worked as a Senior Global Product Manager at Respiratory Motion, Inc. from August 2017 to December 2019. Before joining Respiratory Motion, Inc., Christie worked as a Senior Product Manager, Diagnostics at ResMed from September 2015 to August 2017. Christie also served as a Customer Care Advocacy Manager at CareFusion from July 2014 to July 2015. Prior to that, they held the position of Director of Marketing, Marketing Communications and Product Management at Posey Company from April 2011 to November 2013. Christie's earlier experience includes working as a Senior Global Product Manager at Viasys, Cardinal Health, and CareFusion from 2004 to 2011.
Christie Rose obtained a Master of Business Administration (MBA) degree from the University of California, Irvine - The Paul Merage School of Business from 2004 to 2006. Prior to that, they earned a Master's degree in Exercise Physiology from California State University, Long Beach from 1996 to 1998. In addition to their formal education, Christie Rose obtained a certification as a Certified SCRUM Master from VMEdu Inc. in 2020.
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Timpel Medical
Each and every person is unique. Precision Medicine takes into account individual uniqueness to foster a safer and more effective treatment. Timpel is a leading provider of Electrical Impedance Tomography, covering the needs of all HCPs involved in ventilation and respiratory care. Timpel's multidisciplinairy team is formed from a strong partnership between academia and industry, having a long-term commitment for the succes of its customers, to benefit HCPs, patients and the entire healthcare system. With offices in the Netherlands and Brazil, and an installed base in major European countries, Timpel Enlight 1800 has CE Mark and all required approvals according to European Directives for Medical Devices.