In my current position, I proofread product literature & labels, the company website, specification sheets, certificates of analyses, material reviews & dispositions, white papers. company letters, announcements, statements, and press releases prior to them being posted, sent out, or published. Additionally, I review non-disclosure agreements before company officers signs off on them. I have also been responsible for creating specification sheets and writing material reviews & dispositions as well as company statements and policy positions. I have overall experience as a QA/QC manager in the dietary supplement industry where I was responsible for ensuring that the company I work for became cGMP compliant after the FDAs Final Rules were issued. Additional duties include R&D and Regulatory Compliance & Technical Support.