Michelle T.

Michelle T. has extensive experience in quality control and document review within the pharmaceutical industry spanning over two decades. Currently, Michelle serves as a Document Reviewer at Taro Pharmaceuticals, focusing on method validation and regulatory compliance. Prior roles include Senior Consultant at PharmEng Technology, where responsibilities involved method transfer, data review, and collaboration with QC and QA teams to ensure compliance with health regulations. Michelle's earlier experience at Teva Canada included positions as Quality Control Associate and Stability Associate, contributing to stability testing programs and thorough analyses of OOT/OOS results. Educational qualifications include an Associate's Degree in Chemical Technology from Seneca Polytechnic and additional training at the Academy of Applied Pharmaceutical Sciences.