Pfizer

Procurement

• Lead and co-lead moderately complex projects
• Manage time and resources to meet objectives
• Collaborate with procurement specialists to negotiate contracts
• Oversee category management and corporate services procurement
• Manage the entire sourcing process, from project initiation to supplier management
• Facilitate agreements between teams and drive new concepts
• Achieve annual targets, including savings and Working Capital objectives

Senior Associate, Business Engagement – Sourcing & Enterprise Services

Manager

• Responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within Oncology portfolio
• Clinical development expert for assigned studies maintaining current scientific and clinical knowledge in specific therapeutic and disease area(s)
• Effectively partner with clinical and medical colleagues, clinical operations and other functional lines for successful implementation and execution of clinical trial(s)
• Represent the study team in governance meetings, authors protocols, study level informed consent documents
• Set the clinical data review strategy and lead the team in collection of quality data and review of emerging clinical data and trends
• Analyze the emerging safety profile of the drug, keeping clinical and safety colleagues informed of changes in safety profile

Oncology Clinical Development Scientist – Senior Manager

Director

• Design, lead and execute RWE and epidemiology studies as part of cross-functional IEPs
• Provide subject matter expertise and thought leadership
• Partner with TA RWE/Epi lead and MEG TA Leads
• Work collaboratively to establish & operationalize processes & systems to deliver RWE/Epi studies
• Stakeholder management: build coalitions & develop strong partnerships
• Provide critical assessment to inform asset-specific development strategy
• Prepare study reports and present/publish results of studies at scientific conferences
• Participate in RWE/Epi peer review of study protocols

Director, Oncology RWE Scientist – Secondment, 9 Months

Software Engineer

• Lead the design, development, and deployment of AI agents that automate workflows
• Enhance decision-making and enable intelligent user interactions across the enterprise
• Collaborate with product, data, and engineering teams to align AI priorities with business outcomes
• Mentor junior engineers and ensure knowledge sharing across the team
• Drive the development of automation workflows and APIs that integrate with business tools
• Utilize cloud infrastructure (Azure/AWS/GCP) and MLOps frameworks for continuous delivery
• Ensure code quality, testing, and maintainability through best development practices
• Develop KPIs and success metrics for team deliverables
• Oversee documentation, sprint planning, and backlog prioritization in agile environments

Director, AI Solutions Expert – Agent Developer

• The Area Business Manager (ABM) will be responsible for the supervision and leadership of 9-12 representatives within the area assigned, sales performance of the business portfolio of products, and business knowledge of the area landscape to assess key stakeholders plus future trends within the business marketplace.
• This position will require regular in field and virtual coaching and observation of Field Representatives and frequent customer contact as well as the development of a strong, effective partnership with marketing and channel colleagues.
• The ABM will ensure compliant execution by team members, driving understanding of relevant policies and guidance and advancing a culture of integrity.
• The CARD ABM is responsible for supervising operations of the district to include hiring, live coaching, virtual coaching, representative development, performance management, and the assignment of key "priority" accounts within the medical community, managing 9-12 representatives.

Area Business Manager – Secondment 9-12 Months

• Lead and/or support specific initiatives in the development, implementation, and maintenance of Patient Access/Hub services
• Serve as the subject matter expert to lead the development, innovation, execution, and evolution of the PDPA Hub and patient support program strategies
• Lead and support the development of the access strategic and tactical plans for the Dermatology and other I&I brands
• Lead the execution and maintenance of patient access services
• Lead and manage the Hub/reimbursement services and vendor engagement
• Own budget development and management
• Negotiate and execute contracts with key third-party vendors
• Coordinate with Pfizer Patient Services and USMA colleagues on initiatives
• Leverage data and analytics to identify opportunities to improve all stages of the post Rx patient journey

Director, Patient Services I&I

• Drive Customer Experience innovation by closely working with stakeholders and teams of designers, product leads, and engineers
• Establish clear customer vision, journey maps, and experience roadmaps
• Collaborate closely with stakeholders to align priorities and gather feedback
• Execute the complete CX process from problem definition through MVP delivery
• Conduct AI-accelerated research campaigns synthesizing insights
• Rapidly prototype solutions using Figma AI and design system components
• Coordinate user testing sessions
• Facilitate daily standups and sprint planning sessions ensuring CX perspective is represented

Senior Manager, CX Lead – Commercial Forward Impact Team

Compliance

• Serve as the primary compliance lead for BTx PSOQ, offering strategic guidance on global regulations, industry standards, and internal quality policies.
• Lead the development and implementation of proactive compliance strategies to cultivate a culture of quality and continuous improvement.
• Act as PSOQ compliance lead for regulatory inspections and audits.
• Collaborate with Pfizer corporate auditors on conducting internal audits.
• Lead cross-functional compliance projects across multiple sites with the global PS team to ensure regulatory readiness and reduce risks.
• Collaborate with auditors and stakeholders to influence broader processes and standards.
• Deliver compliance support through risk assessments and advise stakeholders on risk prioritization and remediation strategies.
• Develop and implement risk management strategies for complex, multi-site operations and major capital projects.
• Work with cross-functional teams to implement quality activities and ensure compliance.
• Review SOPs and documents for regulatory or internal requirements.
• Create and maintain quality tools and conduct compliance training.
• Manage quality assessments, risk management, CAPA plans, and/or other compliance documentation.
• Track quality metrics to support audit and inspection readiness to ensure compliance.
• Oversee compliance aspects for major capital projects, ensuring regulatory and internal standards are met throughout all phases of project lifecycles.
• Lead compliance projects that impact multiple sites and contribute to the global PSOQ compliance strategy.
• Partner with key stakeholders for quality reviews, audits, investigations, and process improvement initiatives.
• Drive innovative solutions to enhance efficiency and compliance across GMP operations.

Quality Compliance Lead

• Support Post Approval Changes, initial registrations and/or renewals
• Act as a regulatory expert, advising of regulatory strategy and potential supply constraints, if applicable
• Act as a liaison between CMOs and internal Pfizer functions to ensure timely progression of regulatory activities
• Monitor and notify regulatory submission status, BOH queries, commitments, and approvals
• Support in Compliance Assessment and New Regulations/compendia requirements implementation as required
• Coordinate the collection of supporting documents for Post Approval Changes, initial registration, renewals, BOH queries, and regulatory commitments
• Support license renewals (e.g. GMP Clearance) and Tender applications
• Manage routine complaints for commercial drug product and medical device and combination product

Senior Associate – Contractor Regulatory Operations

• Provide Quality Authority oversight for Core GMP PGS/ERP computer systems
• Lead the Core Solution Support team and manage team resources
• Review and approve GMP related Computer System Standard Operating Procedures
• Provide guidance on aspects of the systems' life cycle defined by Pfizer GMP policies
• Support regulatory or internal audits related to GMP core computer system compliance
• Assist sites in supporting regulatory inspections or internal audits
• Partner with Digital stakeholders for effective delivery and management of core solutions
• Facilitate cross-site/function discussion forums

Senior Manager – Computer Systems Quality Team Lead

• Manage calendars, travel, expenses and correspondence.
• Coordinate meetings, conferences and events.
• Maintain databases and files and prepare monthly reports.
• Process invoices, procurements and contracts in accordance with Pfizer requirements.
• Support onboarding, audits and continuous process improvements.

Regulatory Administrative Assistant – Central and Eastern Europe Cluster

• Responsible for motivating, managing and developing a high performing team of sales professionals
• Driving understanding of relevant policies and guidance and advancing a culture of excellence
• Responsible for the supervision and leadership of 9-12 representatives within the area assigned
• Regular coaching and observation of Neuroscience Health & Science Professionals
• Develop a strong, effective partnership with marketing and channel colleagues
• Ensure full compliance of selling activities for oneself and the team
• Develops and implements strategic plans for the Area Team and overall responsibility for budgets at district level
• Build relationships with customers and key stakeholders

Area Business Manager, Migraine

Risk

• Drive the quality culture in Global Clinical Supply (GCS)
• Provide strategic leadership, oversight, and continuous improvement of key activities integral to Global Clinical Supply business quality and compliance efforts
• Develop talent by ensuring Quality Investigation Leads (QILs) and Inspection Readiness Leads (IRLs) are trained and supported
• Ensure direct reports meet expectations and appropriately escalate risks
• Direct trending and analysis of quality data to proactively identify risks
• Coordinate with GCS and Quality partners to resolve issues
• Foster best practice sharing across teams

Senior Director, GCS Inspection – Risk Management Lead

Brand Manager

• Manages portfolio of products
• Crafts and executes market research to support product portfolio
• Forecasts and tracks portfolio performance
• Seeks and develops business opportunities
• Provides market insights and prepares monthly market insight reports

Country Brand Manager, Biosimilar

Product Manager

• Leads multiple (~2-4) cross functional oncology product teams from pre-clinical candidate nomination (CAN) through Phase 1-2 clinical development and proof of concept (POC) stages
• Drives the effective integration of an end-to-end cross functional molecule strategy and risk mitigation plan
• Ensures delivery of data-driven milestones through successful risk identification and mitigation
• Supports clinical trials and the development strategy for early development assets and leads development programs across multiple functions within Pfizer Oncology
• Represents the program with the external clinical community
• Develops clinical development plan from first in human clinical trial to proof-of-concept, including assessment of appropriate combinations, as well as evaluation of potential predictive and pharmacodynamics biomarker plans
• Oversees early development assets’ development broadly within a specific indication or group of indications
• Manages risk by proactively identifying and resolving issues and developing contingency plans
• Oversees the evaluation of safety, pharmacology, and efficacy data from ongoing and completed studies for early development assets
• Provides leadership to early stage clinical scientists on the clinical study team for Early Development Assets, working in a matrix team environment with other clinicians, statisticians, clinical pharmacologists, translational biologists and regulatory specialists