ENOVIA Developer
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Job Role: ENOVIA Developer Location: Wawatosa, WI Description:Role Descriptions: We are seeking a Senior ENOVIA Developer to support a large-scale, enterprise PLM transformation in the medical technology domain. This is a hands-on technical development role requiring strong expertise in ENOVIA Engineering Central, Supplier Management, Supplier Collaboration, integrations, and data migration. This role is intended for experienced ENOVIA technical developers. Functional users, system administrators, CAD designers, or domain experts without hands-on ENOVIA development experience are not a fit.Key Responsibilities· Design, develop, and extend ENOVIA solutions with a focus on Engineering Central and Supplier Collaboration.· Perform hands-on customization using ENOVIA/3DEXPERIENCE APIs, MQL/TCL, Java, and ENOVIA frameworks.· Implement Supplier Management and Supplier Collaboration capabilities with secure external access models.· Manage document and design data within Engineering Central.· Design and implement integrations between ENOVIA and enterprise systems such as ERP.· Lead and execute PLM data migration activities including data extraction, transformation, validation, and reconciliation.· Collaborate with architects and functional leads to translate requirements into technical solutions.· Troubleshoot complex technical issues and mentor junior developers.Required Technical Skills (Must-Have)· Strong hands-on experience as an ENOVIA Developer in enterprise implementations· Expertise in ENOVIA Engineering Central configuration and customization· Strong experience with Supplier Management and Supplier Collaboration· Hands-on development using MQL, TCL, Java, and ENOVIA frameworks· Deep understanding of ENOVIA data model, lifecycles, policies, and access controlIntegrations & Data Migration· Experience integrating ENOVIA with ERP and downstream systems, including interface design, monitoring, and reconciliation.· Strong experience in PLM data migration including legacy extraction, transformation, bulk loads, validation, and audit readiness.Domain & Regulatory Experience· Experience in medical technology, life sciences, or other regulated industries.· Understanding of regulated supplier collaboration, document control, and audit-ready PLM practices.