Vba developer • sioux falls sd
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]
Outlier helps the world’s most innovative companies improve their AI agents by providing human feedback.We collaborate with leading AI organizations to train Large Language Models (LLMs) to functio...[internal_linking.show_more]
Maximus TCS (Technology and Consulting Services) Internal Job Profile Code: TCS233, T5, Band 8 Job-Specific Essential Duties and Responsibilities: * Provides subject matter proficiency for work des...[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]
Put your Insurance Experience to work – FROM HOME!.Our unique platform provides you with.WHAT YOU’LL LOVE ABOUT WAHVE.We created a welcoming place to work with friendly and professional leadership....[internal_linking.show_more]
Work From Home, Entry Level Data Entry Clerk As A Research Participant.We are looking for people who want to work remotely from home.You'll need an Internet connection and a mobile device or comput...[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)
