> Markdown version of [/jobs/ext/4174294-software-project-manager](https://www.wearedevelopers.com/jobs/ext/4174294-software-project-manager). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Software Project Manager - **Company:** Intellectt, Inc - **Location:** United States (Remote available) - **Experience:** Expert - **Salary:** $114,400 - $135,200 - **Contract:** Permanent contract - **Skills:** Agile Methodology, JIRA, Microsoft Azure, Microsoft Project, Planisware, Scrum Methodology, Software Project Management, Smartsheet, Information Technology - **Published:** October 31, 2026 - **Apply:** https://www.careerbuilder.com/job-details/software-project-manager-in--8dc3f03d-95d6-451b-818c-40ac3653d0f3 ## About the Role Project/Program Management, Project/Program Management, Time Management, Product Development, Cross-Functional, Project Schedule, Medical Equipment, Regulatory Requirements, Budgeting, Schedule Development, * Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related field. * 5+ years of project management experience in regulated medical device or product development environments. * Experience managing projects involving software, systems, and hardware. * Knowledge of medical device design controls, phase-gate processes, and quality management systems. * Familiarity with FDA 21 CFR 820.30 and ISO 13485. * Experience with Agile, SAFe, Lean, or hybrid project management methodologies. * Experience with project schedules, budgets, forecasting, risk management, and earned value management (EVM). * Proficiency with MS Project, Smartsheet, Planisware, Jira, or Azure DevOps. * Strong communication, leadership, organization, and stakeholder management skills. Preferred: Experience with Class II/III medical devices, robotics, navigation systems, or software-enabled products. ## Description We are seeking an experienced Software Project Manager to lead medical device product development projects in a regulated environment. The candidate will manage project schedules, budgets, risks, and cross-functional teams to ensure timely delivery while meeting quality and regulatory requirements., * Develop and manage project plans, schedules, budgets, and milestones. * Track project progress, costs, resources, and deliverables. * Identify and manage project risks, issues, dependencies, and change requests. * Coordinate software, systems, engineering, quality, regulatory, and manufacturing teams. * Lead project meetings and communicate status updates to stakeholders. * Support medical device design controls, documentation, and phase-gate reviews. * Coordinate Agile sprints and cross-functional project activities. * Manage vendor deliverables, resource planning, and project reporting. * Prepare project dashboards and drive issues through resolution. * Support project closure, lessons learned, and transition activities.