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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in strategic learning and capability development, with a strong focus on regulatory compliance, quality systems, and performance consulting within the pharmaceutical industry. Proven ability to lead cross-functional initiatives and influence stakeholders at all levels without direct authority.
Highest-signal resume keywords
Pharmaceutical Manufacturing KnowledgeRegulatory Compliance ExpertiseLearning Strategy DevelopmentProcess GovernanceStakeholder Engagement
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality SystemsGxP RequirementsPerformance ConsultingInstructional DesignCurriculum Lifecycle ManagementData AnalysisProcess ImprovementTraining DevelopmentRisk AssessmentOrganizational Capability
Soft Skills
Executive CommunicationInfluencing SkillsCoaching and MentoringAnalytical ThinkingProblem Solving
Industry Keywords
Quality Management ProcessesPersonnel QualificationTraining ManagementContinuous ImprovementDigital StrategyCross-Functional LeadershipGlobal InitiativesStakeholder AlignmentRegulatory Inspection SupportOrganizational Transformation
About the role
Key responsibilities & impact- Serve as a strategic learning and capability advisor to QSEO leadership across the Americas and broader PGS network
- Translate business strategy, quality priorities, regulatory expectations, emerging technologies, and workforce needs into scalable learning and organizational capability solutions
- Serve as Local Process Owner for Personnel and Training Management for Above-Site QSEO
- Represent QSEO on the L2 Personnel and Training Management Process Centric Team and serve as regional L2 PCT Leader and proxy for the Global Process Owner
- Lead design, governance, deployment, performance monitoring, and continuous improvement of Personnel and Training Management processes
- Provide oversight for personnel qualification, job descriptions, curricula, training requirements, documentation, and curriculum lifecycle management
- Establish and interpret process-health, performance, effectiveness, and compliance metrics
- Lead Learning Needs Assessments and approve learning strategies for assigned L2 Quality Management Processes
- Develop scalable training, learning, knowledge-management, and performance-support solutions using contemporary instructional design and performance-consulting practices
- Partner with Global Process Owners, subject matter experts, Learning colleagues, Digital, Process Owners, and other stakeholders
- Monitor regulatory expectations, quality trends, inspection outcomes, industry developments, and emerging technologies
- Provide expert guidance before, during, and after regulatory inspections
- Lead complex cross-functional, cross-site, cross-regional, and global initiatives
- Influence the digital strategy and roadmap for Personnel and Training Management
- Coach, mentor, and provide technical leadership without direct supervisory responsibility
- Represent Pfizer as a subject matter expert at external pharmaceutical, quality, regulatory, learning, or industry forums
- Travel up to 10% and periodically work in manufacturing or controlled environments
Requirements
What you’ll need- Applicant must have a bachelor's degree with 8 years of experience; OR a master's degree with 7 years of experience; OR a PhD with 5+ years of experience
- Significant experience operating as a senior individual contributor with accountability for complex, cross-functional, regional, or global programs, processes, or outcomes
- Strong knowledge of pharmaceutical manufacturing, quality systems, regulatory compliance, and GxP requirements
- Demonstrated ability to translate business and organizational priorities into strategic learning, capability, process, or performance solutions
- Demonstrated ability to operate independently in complex and ambiguous environments, integrate multiple perspectives, assess risk and trade-offs, and determine appropriate recommendations or courses of action
- Demonstrated success leading significant initiatives across functional, organizational, or geographic boundaries
- Demonstrated ability to establish direction, align stakeholders, and drive results through expertise and influence without direct reporting authority
- Strong strategic, analytical, and critical-thinking capabilities, including the ability to synthesize business information, quality signals, performance data, and external trends to identify systemic risks and opportunities
- Demonstrated expertise in organizational capability, learning strategy, performance consulting, process governance, quality systems, operational excellence, or related disciplines
- Strong executive communication, consultation, and influencing skills, including demonstrated effectiveness engaging Senior Director and Vice President-level stakeholders
- Demonstrated ability to constructively challenge established approaches and develop innovative, sustainable, and scalable solutions
- Ability to establish credibility as a subject matter expert with senior internal and external stakeholders
- Strong understanding of evolving regulatory and industry expectations affecting personnel qualification, training, knowledge management, and organizational capability
- Demonstrated ability to coach, mentor, and build the capability of others without formal people-management responsibility
- Demonstrated effectiveness operating across functions, cultures, geographies, and organizational boundaries in a highly matrixed environment
- Must be authorized to be employed in the U.S. by any employer
- Requires permanent work authorization in the United States
- U.S. work visa sponsorship is not available for this role now or in the future
- Ability to travel, as required, to Pfizer sites and other business locations
- Nice-to-have qualifications include a relevant bachelor's or master's degree, 10+ years of relevant experience, advanced instructional systems design and adult learning knowledge, regulated pharmaceutical or GxP training-process experience, global or regional network experience, organizational capability or process-transformation leadership, analytics/technology/automation experience, regulatory inspection support, and external industry participation
Benefits
Comp & perks- Global Performance Plan with a bonus target of 20.0% of base salary
- Share based long term incentive program
- 401(k) plan with Pfizer Matching Contributions
- Additional Pfizer Retirement Savings Contribution
- Paid vacation, holiday and personal days
- Paid caregiver/parental and medical leave
- Medical, prescription drug, dental and vision coverage
- Relocation assistance may be available based on business needs and/or eligibility
