Our client is a gene therapy CDMO focused on viral vector process and analytical development, and they are in need of a Project 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