Principal Supplier Quality Engineer @ From May 2015 to Present (6 months) Corporate Manager QMS & Labeling @ From February 2015 to May 2015 (4 months) Manager, Corporate Labeling @ From December 2013 to February 2015 (1 year 3 months) Largo, FLSenior Quality System Specialist @ From July 2012 to December 2014 (2 years 6 months) Largo, FloridaSenior Corporate Auditor @ From 2008 to January 2012 (4 years) Quality System Engineer @ From 2007 to 2008 (1 year) Quality Engineer @ From October 2004 to November 2007 (3 years 2 months) Research Chemist @ From May 2003 to October 2004 (1 year 6 months)

B.S., Chemistry @ Quinnipiac University From 1999 to 2003 Amanda Davis is skilled in: ISO 13485, 21 CFR Part 11, 21 CFR 820, Quality Auditing, Six Sigma, Medical Devices, V&V, Design Control, CAPA, FDA, CE marking, Manufacturing, 21 CFR, Supplier Quality, Regulatory Affairs, Sterilization, Quality Control, GMP, Quality System, Sop, Validation, ISO 14971, Lean Manufacturing, FDA GMP, Continuous Improvement, ISO, Biomedical Engineering, Change Control, DMAIC, Medical Device Directive, FMEA, Quality Assurance, Regulatory Submissions, Quality Management, PMA, Root Cause Analysis