Location: Brookhaven,NY, USA
Description:Amneal Pharmaceuticals is seeking a skilled JD Edwards Manufacturing and Supply Chain IT Specialist to join our dynamic IT team. This role will focus on the design, development, implementation, and support of JD Edwards EnterpriseOne (JDE) ERP solutions in the manufacturing and supply chain domains. The ideal candidate will collaborate with various business units to ensure the seamless integration of manufacturing, supply chain, and distribution operations with the JD Edwards system, driving process improvements and operational efficiency.Essential Functions:ERP Implementation and Support: Lead the implementation, customization, and support of JD Edwards EnterpriseOne (JDE) modules specific to Manufacturing, Supply Chain Management (SCM), Inventory Management, Procurement, and Sales Order Management. Work with business users to gather requirements, analyze workflows, and design solutions that align with operational needs. Develop and maintain JDE configurations, security settings, and process workflows, ensuring optimized use of ERP capabilities.System Customization and Development: Develop and implement custom applications, reports, and workflows using JDE toolsets like Orchestrator, E1 Pages, and BI Publisher. Customize the JD Edwards EnterpriseOne modules to meet the unique requirements of the pharmaceutical industry, especially around compliance and traceability. Support the development of interfaces for seamless integration with third-party systems (e.g., CRM, LIMS, shipping systems).Process Improvement and Optimization: Partner with manufacturing, supply chain, and distribution teams to streamline operations, improve efficiencies, and reduce costs by leveraging JDE system capabilities. Implement best practices for manufacturing processes such as production scheduling, work orders, bill of materials (BOM) management, and shop floor control. Develop and enhance supply chain processes, including demand planning, procurement, inventory control, and logistics.Compliance and Validation: Ensure that all JDE configurations and customizations comply with industry standards, regulatory requirements, and FDA guidelines. Collaborate with quality assurance teams to support validation processes, documentation, and testing for JDE ERP systems in compliance with pharmaceutical industry regulations.Integration and Data Management: Oversee integration between JDE and other enterprise systems, including MES (Manufacturing Execution Systems), SCADA, and warehouse management systems (WMS). Collaborate with IT and data analytics teams to provide real-time data insights for KPIs, inventory levels, production performance, and other critical business metrics. Ensure data accuracy, system reliability, and adherence to GMP (Good Manufacturing Practice) and 21 CFR Part 11 requirements.Training and Support: Provide hands-on training and support to end users in various departments on JDE system functionalities. Troubleshoot issues, provide system updates, and ensure smooth operation of the JDE platform, focusing on manufacturing and supply chain activities. Coordinate with external vendors and technical consultants to resolve system issues, implement upgrades, and support JDE version upgrades.Travel expectations of approximately 15-25% to support other sites, including New Jersey.