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Erin Kriebel has been in the quality assurance and regulatory affairs field since 2005. Erin began their career at GlaxoSmithKline as a Biopharmaceutical Manufacturing Associate. In 2008, they moved to MD Biosciences, Inc. as a Quality Systems Specialist/Manager. In 2011, they joined SurModics as a Quality Engineer (Manufacturing). In 2012, they moved to Siemens Healthcare as a Quality Engineer (Regulatory Affairs). In 2018, they joined Camber Spine Technologies as Director of Quality. Most recently, in 2020, they joined Vitara Biomedical as Director of Quality.

Erin Kriebel completed a Bachelor of Science in Biology and a Bachelor of Science in Crime, Law and Justice - Forensic Science from Penn State University between 2001 and 2005. Erin also holds an ISO 13485:2016 Lead Auditor certification from BSI.