<p>Our client in the Washington, DC area is seeking an experienced <strong>Program Manager</strong> with a strong background in the <strong>medical device, biotech, or regulated healthcare technology</strong> 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.</p><p>You’ll oversee program planning, execution, timelines, and stakeholder communication while supporting product development, quality initiatives, and regulatory alignment.</p><p><br></p><p><strong>Key Responsibilities</strong></p><ul><li>Lead end‑to‑end program management for medical device initiatives, from planning through execution</li><li>Coordinate cross‑functional teams including engineering, R&amp;D, quality, regulatory, and operations</li><li>Develop and maintain program timelines, milestones, budgets, and risk mitigation plans</li><li>Ensure compliance with FDA, ISO, and other regulatory standards</li><li>Facilitate communication between internal teams, leadership, and external partners</li><li>Track program performance and provide reporting, dashboards, and status updates</li><li>Support product development lifecycle activities, including design reviews and documentation</li><li>Identify process improvements to enhance efficiency and program outcome</li></ul><p><br></p>

<p><strong> Required Skills &amp; Experience</strong></p><ul><li>5–8+ years of program or project management experience</li><li>Background in <strong>medical devices, biotech, diagnostics, or healthcare technology</strong></li><li>Strong understanding of regulatory frameworks (FDA, ISO 13485, QMS)</li><li>Proven experience managing complex, multi‑phase programs</li><li>Excellent communication, stakeholder management, and organizational skills</li><li>Proficiency with project management tools (Smartsheet, MS Project, Jira, etc.)</li><li>Ability to work in fast‑paced, highly regulated environments</li></ul><p><strong>Preferred Qualifications</strong></p><ul><li>PMP, PgMP, or similar certification</li><li>Experience with product development lifecycle (PDLC) or design controls</li><li>Familiarity with risk management methodologies (FMEA, CAPA, etc.)</li><li>Background working with cross‑functional technical teams</li></ul><p><br></p>

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