What are the responsibilities and job description for the Project Manager position at S4 Analytics LLC?
About the Role:
Our client, a leading gene therapy Contract Development and Manufacturing Organization (CDMO) specializing in viral vector process and analytical development, is seeking an experienced Program Manager. This role involves overseeing multiple cross-functional projects within Process Development, Analytical Development, Quality Control, and Operations teams, ensuring seamless integration and successful project delivery.
Key Responsibilities:
- Project Leadership: Independently lead and manage at least 4 projects simultaneously, ensuring on-time, on-budget delivery.
- Planning & Scheduling: Develop and maintain RAID Logs and Gantt charts; monitor and track activities associated with budgets, invoicing, timelines, scope, alignment, and priorities.
- Cross-Functional Collaboration: Work closely with non-GMP teams, including Process Development, Analytical Development, Quality Control, and Operations, to ensure project success.
- Communication: Serve as the primary point of contact for internal and external stakeholders, providing regular updates and addressing any issues promptly.
Technical Requirements:
- Bachelor's degree in a relevant field.
- Minimum of 5 years of experience in biotech/pharmaceutical cross-functional team program or project management.
- Direct experience in a CDMO environment or strong external manufacturing project management experience with sponsor companies.
- Proficiency in Microsoft Office Suite and project management software (e.g., Smartsheet).
- Excellent communication, interpersonal, negotiation, and business skills.
Preferred Qualifications:
- Experience with Adeno-associated virus (AAV) vectors, biologics, or gene therapy.
- Prior laboratory or scientific/research background.