Description

You will lead cross-functional client-facing and internal projects at a Syracuse-based biologics CDMO, ensuring on-time, on-budget delivery. You'll establish project governance, manage stakeholder relationships, and drive continuous improvement to support long-term site objectives.

Requirements

• Bachelor's degree in Engineering, Life Sciences, or related technical field
• 5-10 years of project management experience in matrixed organization
• 3-5 years CDMO industry experience with cGMP or technical transfer projects
• Strong understanding of biologics manufacturing and regulatory requirements
• Financial acumen including cost estimation and invoicing

Responsibilities

• Lead strategic client-facing projects from initiation through closeout
• Develop and manage detailed project plans with critical path and milestones
• Serve as primary client liaison for communication, scope management, and change orders
• Identify and resolve project risks and issues, escalating when needed
• Maintain PMO governance tools: metrics, dashboards, risk logs, KPI reporting