Kayla Bowden is a seasoned professional in the pharmaceutical compliance field, currently serving as a Senior Compliance Specialist at Cadista Pharmaceuticals since June 2017. In this role, Kayla manages the Stability Program, writes and reviews Annual Product Reviews (APRs), conducts deviation investigations, and oversees quality control test method revisions along with associated SAP updates. Kayla is also responsible for reviewing and approving Standard Operating Procedure (SOP) revisions, change controls, deviations, and Corrective and Preventive Actions (CAPAs), as well as vendor and material qualification. Additionally, Kayla has played a key role in the implementation of MasterControl and is recognized as a subject matter expert in TrackWise, MasterControl, and ComplianceWire. Previously, Kayla held various compliance and administrative positions with Accohannock Indian Tribe Inc. from June 2010 to 2015. Kayla earned a Bachelor of Science degree in Biology from the University of Maryland Eastern Shore between 2012 and 2016.