Amber Luker

Amber Luker is a seasoned regulatory affairs professional with extensive experience in the medical device industry. Currently serving as a Principal Regulatory Affairs Specialist at Medtronic since February 2020, Amber's focus is on renal denervation, building on a solid background with the Ellipsys pAVF System and various stent systems. Previously, at Abbott from May 2018 to February 2020, Amber managed regulatory projects for 3-D cardiac mapping systems and developed Technical Files and Pre-Submissions. Amber's expertise further extends from time at ACIST Medical Systems (November 2015 - May 2018), where responsibilities included regulatory work on intravascular ultrasound systems, to a senior regulatory role at Boston Scientific (January 2009 - November 2015), dealing with high voltage leads and implantable defibrillator systems. Earlier in the career, Amber also contributed to technical writing and human tissue regulation at WuXi AppTec. Amber holds a Bachelor of Science degree in Biological Sciences from Northern Illinois University.