- 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)
- Develop and update detailed project plans, timelines, budgets and resource allocations
- Lead weekly project team meetings to communicate project status, updates and milestones to the project team and executive management.
- Collaborate with internal stakeholders and external partners
- Drive accountability for project deliverables
- Identify risks and implement effective mitigation strategies
- Ensure project documentation is complete, current and stored appropriately
- Utilize electronic project management tools to track progress
Experience & Qualifications:
- 3+ years of relevant work experience
- Experienced project manager in a regulated life sciences company (human tissue preferred, or medical device, biologics, pharmaceuticals)
- Six Sigma Green Belt preferred
- Ability to work independently and manage multiple stakeholders
- Knowledge of project management frameworks and best practices