Moved to the Quality unit as a Senior Quality Engineer in 2014. Became a Certifed CQE thru ASQ in 2014 and a Certified CQA thru ASQ in 2015. Currently work in both the laboratory and manufacturing settings.Documentation Specialist for GMP Pharmaceutical manufacturing. (Batch Records, Specifications, Methods, Formulation Tickets, Supplier Selection)Quality Liaison for the lab to work closely with the quality unit and to keep the lab in compliance. Represent lab in internal and external audits.Lead process engineer for process simulation work for sterile product.28 years experience in Pharmaceutical Research and Development in the areas of Transdermal, Inhalation, and Microneedle Delivery Systems
Listed skills include Gmp, Drug Delivery, Fda, Formulation, and 17 others.