Job Description

Our client is a gene therapy CDMO focused on viral vector process and analytical development, and they are in need of a Program Manager for a 12-month assignment.

Responsibilities :

• Project planning, development, scheduling execution, monitoring and tracking activities associated with budgets, invoicing, timelines, scope, alignment and priorities for Process Development, Analytical Development, Quality Control, and Operations teams.
• Development of RAID Logs and Gantt charts
• Individually lead and manage at least 4 projects simultaneously

Technical Requirements :

• BS Degree minimum; 5+ years of biotech/pharmaceutical cross-functional team program or project management experience
• Direct CDMO experience as a PM, or strong external manufacturing PM experience with sponsor companies.
• Demonstrates previous experience working with non-GMP teams: Process Development, Analytical Development, Quality Control, and Operations teams.
• Excellent communication, interpersonal, negotiation, and business skills
• Solid Microsoft Office and project management software skills (Smartsheet)

Preferred Qualifications :

• Adeno-associated virus vectors (AAV), Biologics, or Gene Therapy experience
• Prior lab or scientific/research background
• SAP experience

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