PMO Sr. Project Manager

About this role

Use Your Power for Purpose

At Pfizer, our mission is to cultivate a best-in-class culture of continuous improvement and project management, empowering colleagues and streamlining processes. Whether managing projects or collaborating with others, your role in this team is crucial in simplifying and accelerating our work. This enables us to deliver groundbreaking innovations that transform patients' lives. Your contributions will make our operations more efficient and effective, driving us towards achieving our goal of making a significant impact on healthcare. Join us in this mission to inspire excellence and facilitate breakthroughs that truly matter.

What You Will Achieve

In this role, you will:

• Lead or co-lead moderately complex projects, effectively managing time and resources • Apply program management discipline and business acumen to contribute to departmental and site goals.   • Resolve moderately complex problems and develop new options, guided by policies in non-standard situations • Operate independently in ambiguous situations and determine objectives of assignments • Review your own work and seek directional review from others, potentially reviewing colleagues' work in a mentor role • Oversee operational aspects of ongoing improvement projects, acting as a liaison between Project Team and Line Management • Support programs by reviewing project status, budgets, schedules, and preparing comprehensive status reports • Identify project issues and develop resolutions to meet productivity, quality, and client satisfaction goals • Guide operational teams in managing projects, forecasting resource requirements, and identifying areas for improvement in products, processes, or services

Here Is What You Need (Minimum Requirements)

• BA/BS with at least 4 years of experience or MBA/MS with at least 2 years of experience or PhD/JD with any years of experience or associate's degree with at least 8 years of experience or high School Diploma (or Equivalent) with at least 10 years of relevant experience • Demonstrated experience in commercial/customer-facing roles across the business • Experience in leading and coordinating assigned technical transfer projects and work packages. • Knowledge of the workings of pharmaceutical manufacturing and associated processes • Experience in developing, maintaining, and proactively managing integrated project schedules and monitoring project milestones, risks, issues, and dependencies. • Experience in cross-functional team meeting management and driving accountability for deliverables. • Experience working in Pharmaceutical Good Manufacturing Practices (cGMP) environment • Familiarity with Pharmaceutical Sciences infrastructure • Proactive and has a creative entrepreneurial attitude with evidence of ability to execute key projects • Excellent verbal and written communication skills • Proficiency with computer and software applications

Bonus Points If You Have (Preferred Requirements)

• Master's degree with specific experience in managing pharmaceutical, technical, or medical device projects and clinical programs • Minimum 3 years of hands-on project management experience preferably in a regulated manufacturing or pharmaceutical environment with demonstrated experience in project management and cross-functional leadership. • Knowledge and certification in project management methodologies • Strong leadership and team management skills • Ability to work collaboratively in a cross-functional team environment • Ability to adapt to changes in business strategies and operational imperatives • Ability to mentor and guide junior colleagues • Proficiency with project management platforms and tools (e.g., MS Project, Planner). • Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

PHYSICAL/MENTAL REQUIREMENTS

• Physical requirements include sitting, standing, bending, or walking.

• Ability to write general correspondence, technical reports, perform mathematical calculations, data analysis, problem solving. 

• Ability to remain organized and positive in ambiguous and rapidly changing situations. • Ability to analyze data from detailed schedule and risk management tools. • Interface effectively with multiple stakeholder groups.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

• Limited travel required.  • Non-standard work hours, support of global conference calls, 24/7 manufacturing, etc. required when needed, though not typical of weekly requirements.

Work Location Assignment: Hybrid Last Date To Apply: September 15, 2026 
The annual base salary for this position ranges from $99,200.00 to $165,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.



 Relocation assistance may be available based on business needs and/or eligibility. 
 Candidate

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