Mark Jackson

Mark Jackson possesses extensive experience in the pharmaceutical industry, particularly in regulatory affairs, validation, and quality control. From August 2003 to June 2005, Mark held various roles at Dechra Pharmaceuticals PLC, including Product Development Coordinator and Validation Coordinator, focusing on validation requirements and developing validation policies. Subsequent positions included Regulatory Affairs Specialist and Manager, providing comprehensive regulatory support for veterinary pharmaceutical projects to ensure compliance with FDA/CVM regulations. Mark's expertise extends to pharmaceutical development coordination and analytical processes within quality control, utilizing advanced analytical techniques under GLP/GMP conditions. Currently serving as Senior Regulatory Affairs Manager at Dechra, Mark continues to leverage a robust background that includes prior experience as Associate Director of Regulatory Affairs at Dales Pharmaceuticals Limited. Mark holds a Bachelor’s Degree in Biomedical Sciences from the University of Sunderland.