Senior PMO Project Leader – Hybrid, Global Programs

Pfizer; Kansas; Hybrid; USD 99,000 - 165,000; Full time

Job summary

Pfizer is seeking a Senior Project Manager to lead moderately complex projects, coordinating with cross-functional teams to meet regulatory and quality milestones. This role emphasizes program discipline, resource forecasting, and proactive problem-solving in a cGMP environment.

The position requires strong communication skills, extensive pharmaceutical manufacturing knowledge, and experience guiding schedules and dependencies. Hybrid work options available in the United States.

Qualifications

• Demonstrated experience leading and coordinating technical transfer projects and work packages.
• Experience in commercial/customer-facing roles across the business.
• Knowledge of pharmaceutical manufacturing and associated processes.
• Experience in integrated project schedules with milestones, risks, issues and dependencies.
• Experience in cross-functional team meeting management and accountability for deliverables.

Responsibilities

• Lead or co‑lead moderately complex projects, managing time and resources.
• Apply program management discipline to contribute to department and site goals.
• Resolve moderately complex problems and develop new options within policy.
• Operate independently in ambiguous situations and set objectives.
• Review work and mentor colleagues as needed.
• Oversee operational aspects of ongoing improvement projects and liaise with lines.
• Support programs by reviewing status, budgets, schedules, and reporting.
• Identify issues and develop resolutions to meet productivity and quality goals.

Skills

Project management

Cross-functional leadership

Communication skills

Scheduling & risk management

MS Project / Planner

Education

BA/BS or higher with relevant experience

Tools

MS Project

Planner

Job description

Pfizer is seeking a Senior Project Manager to lead moderately complex projects, coordinating with cross-functional teams to meet regulatory and quality milestones. This role emphasizes program discipline, resource forecasting, and proactive problem-solving in a cGMP environment.

The position requires strong communication skills, extensive pharmaceutical manufacturing knowledge, and experience guiding schedules and dependencies. Hybrid work options available in the United States.