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Our client in the Washington, DC area is seeking an experienced Program Manager with a strong background in the medical device, biotech, or regulated healthcare technology space. This role is ideal for a strategic, detail‑driven leader who can manage complex programs, coordinate cross‑functional teams, and ensure compliance within a highly regulated environment. You’ll oversee program planning, execution, timelines, and stakeholder communication while supporting product development, quality initiatives, and regulatory alignment.
Job Responsibility:
Lead end‑to‑end program management for medical device initiatives, from planning through execution
Coordinate cross‑functional teams including engineering, R&D, quality, regulatory, and operations
Develop and maintain program timelines, milestones, budgets, and risk mitigation plans
Ensure compliance with FDA, ISO, and other regulatory standards
Facilitate communication between internal teams, leadership, and external partners
Track program performance and provide reporting, dashboards, and status updates
Support product development lifecycle activities, including design reviews and documentation
Identify process improvements to enhance efficiency and program outcome
Requirements:
5–8+ years of program or project management experience
Background in medical devices, biotech, diagnostics, or healthcare technology
Strong understanding of regulatory frameworks (FDA, ISO 13485, QMS)