Coldfusion developer • syracuse ny
Role Overview** Mercor is partnering with leading AI labs on **Project Atlas** — an initiative to build realistic enterprise environments that frontier AI agents are trained and evaluated in.We're ...[internal_linking.show_more]
This position is critical for local payor extracts and at-risk contracts such as Excellus, Fidelis and Molina.Position is regional and supports both St.We, St Joseph’s Health and Trinity Health, se...[internal_linking.show_more]
Role Overview We’re hiring Software Engineers to build and ship apps for Mercor’s RL Studio platform.The role involves developing MCP servers and sometimes BUAs, integrating real software into sand...[internal_linking.show_more]
PYRAMID MANAGEMENT GROUP, LLC .SPECIALTY LEASING REPRESENTATIVE.Pyramid Management Group, LLC, headquartered in Syracuse, NY, is the largest privately held developer, owner and manager of retail sh...[internal_linking.show_more]
As a Senior SQL Engineer, you will work remotely on an hourly paid basis to review AI-generated SQL queries, database designs, and data-processing logic, as well as generate high-quality reference ...[internal_linking.show_more]
Web Developer Job Duties: Regular exposure to business stakeholders and executive management, as well as the authority and scope to apply your expertise to many interesting technical problems.Cand...[internal_linking.show_more]
The Best Teams are Created and Maintained Here.The Business Developer (BD) works to improve BrightView’s market position and achieve profitable financial growth.This role helps to achieve long-term...[internal_linking.show_more]
Mercor is partnering with leading AI labs on Project Atlas — an initiative to build realistic enterprise environments that frontier AI agents are trained and evaluated in. We're seeking experienced medical-device professionals from Fortune 500 device manufacturers (e.g., Medtronic, Stryker, Boston Scientific, Abbott, J&J MedTech, GE Healthcare) to recreate the digital workspaces they run every day and design the tasks that genuinely challenge state-of-the-art AI. You'll bring your expertise in device R&D, regulatory affairs, quality, manufacturing, or clinical affairs to build a high-fidelity environment that mirrors the tools, files, and cross-functional workflows of a regulated medical-device enterprise — and then author tasks grounded in the programs you actually run today. Key Responsibilities - Build a realistic digital workspace centered on the Drive folders you use day-to-day — the design history files, regulatory submissions, DHF / DMR documents, risk-analysis matrices, validation protocols, CAPA records, and email threads that reflect how you actually organize your work — with some representation of the platforms that support it (e.g., ANSYS Fluent simulations, Siemens Opcenter MES, DocuSign)
