Seeking highly motivated scientists to perform HPLC or GC method development and validation. Must be able to work in a cGMP environment. Must be able to write development plans, validation protocols, and technical reports ready for regulatory scrutiny. Responsible for project management and direct communication with client contacts. Requires outstanding writing, documentation, and organizational skills. A minimum 3 years HPLC or GC development and validation experience preferred. Experience with FDA, USP, and ICH guidelines is expected. Minimum of B.S. degree in Chemistry or closely related field is required.