ºÝºÝߣshows by User: MindyWeir1 / http://www.slideshare.net/images/logo.gif ºÝºÝߣshows by User: MindyWeir1 / ºÝºÝߣShare feed for ºÝºÝߣshows by User: MindyWeir1 https://cdn.slidesharecdn.com/profile-photo-MindyWeir1-48x48.jpg?cb=1645578343 Accomplished Quality Control / Quality Systems Professional in the pharmaceutical industry with a formal education in analytical chemistry and experience in pharmaceutical analysis, stability program and laboratory management, technology transfer, quality systems, manufacturing documentation, product release, and internal / external auditing. •Over 15 years experience in a cGMP (21 CFR Part 210 and 211) environment ensuring safety, identity, strength, purity, and quality; •Five years as a manager of laboratory staff ranging from 9-13 people; •Over nine years managing QC/Stability programs for commercial product and clinical trial materials; •Diverse analytical skills ranging from ba http://www.interceptpharma.com/