CONMED
Tina Mornak is an accomplished Regulatory Affairs Manager at CONMED Corporation since November 2019, leading initiatives for compliance with the EU MDR 2017/745 by developing technical documentation templates and managing project timelines for notified body submissions. Prior experience includes a progression through various titles at Stryker from March 2012 to October 2019, where Tina served as Staff Regulatory Affairs Specialist, Senior Regulatory Affairs Specialist, Regulatory Affairs Specialist, and Regulatory Affairs Associate. Tina's career began as a Regulatory Affairs Engineer at ZOLL from January 2010 to March 2012. Tina holds a Bachelor of Science degree in Bioengineering from the University of Pittsburgh, earned between 2003 and 2007.
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CONMED
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ConMed Corporation is a global medical technology company that specializes in the development and sale of products and services that allow the physician customers to deliver high quality care and as a result, enhanced clinical outcomes for their patients.