We are seeking a dynamic and detail-oriented Project Manager to support strategic initiatives within the T1D program, with a primary focus on external manufacturing and supply chain operations. This role will drive cross-functional collaboration across Operations, MSAT, Regulatory, and Quality to ensure successful execution of tech transfers, operational excellence, and lifecycle management projects.
Key Responsibilities
- Collaborate with functional leads to develop and maintain detailed project plans
- Identify interdependencies and critical path activities to ensure timely execution
- Facilitate process mapping and scenario planning workshops to address challenges
- Track milestones, decision points, and drive accountability across project teams
- Communicate project status, risks, and mitigation strategies to stakeholders
- Maintain project documentation including agendas, minutes, decision logs, and risk registers
- Update dashboards and project tracking tools to reflect current status and actions
- Ensure all activities are conducted in accordance with SOPs and applicable GxP requirements
- Support additional strategic projects based on program needs and individual bandwidth
Requirements
- Bachelor’s degree in Engineering, Life Sciences, or related field
- Minimum of 6 years of experience managing cross-functional, technically complex projects in the biopharmaceutical industry
- Strong working knowledge of GMPs, biotechnology operations, and project management methodologies
- Proven ability to manage multiple priorities in a matrixed environment
- Proficiency in Microsoft Office Suite (Project, PowerPoint, SharePoint, Word, Excel, Outlook)
- Core-level experience with Smartsheet or similar project management tools
- Excellent written and verbal communication skills, including presentation and facilitation
- Strong analytical and problem-solving abilities with both detail orientation and strategic perspective
Benefits
- Contract position with possible extension