I have written hundreds of training guides, operating procedures, writing seminars and workshops. I am experienced in document control and management, especially within the context of GLP and the Biotech industry. I have also served as a NEBAALAS lecturer on technical writing, communication and document formatting.I am deeply familiar with protocol and compliance data review, and the importance of creating well-crafted material in GLP organizations subject to audit by the FDA, USDA, EPA, OECD and other agencies. These skills have been cultivated by my time as a regulated document writer and specialist certified in process re-engineering. I have worked extensively with training teams in helping them draft clearer training documents for smoother on-boarding and faster learning for new technicians. My extensive editorial experience has allowed me to serve as a document owner for entire departments. I have been relied upon to catch errors that would otherwise make it into official or published material and documentation.It is for me a genuine delight to take good documentation and make it great, and to then take great documentation and make it perfect. I have a personal love for writing, communication and storytelling of all sorts. Any opportunity to be an articulate voice for another is a pleasure. I enjoy crafting precise material across multiple platforms, whether that be written or spoken.