Syngenta Group - Greensboro, NC
posted 3 months ago
In this role, you will be working cross-functionally with various departments to ensure the timely delivery of submission packages that support North American (NA) registration activities for the Environmental Protection Agency (EPA) and Pest Management Regulatory Agency (PMRA). This includes handling submissions for new active ingredients, new products, label amendments, and Registration Review processes. Your responsibilities will involve the preparation of essential documentation such as cover letters, application forms, and data matrices that are crucial for inclusion in submission packages aimed at product registrations. You will actively participate in Regulatory Portfolio teams and engage in activities that support and drive strategic submission planning, preparation, and tracking of regulatory analytics. A key aspect of your role will be ensuring the quality and accuracy of information entered into Regulatory databases, including Veeva, Sharepoint, and Smartsheet, while also focusing on continuous improvement in these processes. You will be expected to develop a comprehensive understanding of various laws related to pesticide regulation in North America, particularly the US EPA's Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) and the relevant sections of the Code of Federal Regulations (40CFR). Additionally, you will prepare written communications, which may include presentations, graphics, spreadsheets, and other forms of information. Your role will also involve searching for, integrating, and extrapolating regulatory and scientific data/information to support the submission processes. This position is based in Greensboro, NC, and follows a hybrid work schedule, allowing for a blend of in-office and remote work.