Ana Rita Pereira is a Senior QC Technical Specialist with extensive experience in quality control within the pharmaceutical industry. Ana Rita has held various leadership positions, overseeing teams responsible for the validation of analytical methods in process chemistry development and drug product development. Ana Rita also has experience as an Analytical Chemist, contributing to method validation and data review. Ana Rita's expertise includes QC improvement, developing procedures, coordinating training sessions, and ensuring compliance with cGMP standards.Ana Rita's dedication to high quality levels and continuous improvement is evident throughout their career.
June 1, 2021 - present
May, 2019
October, 2018
June, 2016
August, 2014
January, 2008