Signage Project Manager In Office Jobs in Kansas

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

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.

• 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

• 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

• 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, includingrisk management and ethical use

• 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.

• 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

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.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

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.

• 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

• 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

• 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, includingrisk management and ethical use

• 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.

• 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

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.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibi