<p><strong>Essential Duties & Responsibilities</strong></p><ul><li>Develop the Master Project Plan and sub plans as needed to support the development of the facility and related processes in accordance with industry standards (including AATB, FDA, cGMP)</li><li>Develop and update detailed project plans, timelines, budgets and resource allocations</li><li>Lead weekly project team meetings to communicate project status, updates and milestones to the project team and executive management.</li><li>Collaborate with internal stakeholders and external partners</li><li>Drive accountability for project deliverables</li><li>Identify risks and implement effective mitigation strategies</li><li>Ensure project documentation is complete, current and stored appropriately</li><li>Utilize electronic project management tools to track progress</li></ul><p><br></p>

<p><strong>Experience & Qualifications</strong></p><ul><li>3+ years of relevant work experience</li><li>Experienced project manager in a regulated life sciences company (human tissue preferred, or medical device, biologics, pharmaceuticals)</li><li>Six Sigma Green Belt preferred</li><li>Ability to work independently and manage multiple stakeholders</li><li>Knowledge of project management frameworks and best practices</li></ul>

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