Jobs at Pfizer

Leads strategy, delivery, governance, adoption, and lifecycle management for agentic AI products across Pfizer’s regulated manufacturing network. Defines use cases, roadmaps, evaluation frameworks, guardrails, success metrics, and value-realization models while partnering with manufacturing, engineering, data, quality, cybersecurity, and business teams. Oversees pilots, production deployment, monitoring, continuous improvement, responsible AI, and scaling of intelligent manufacturing capabilities.

Build, prototype, evaluate, deploy, and improve agentic AI products for Pfizer’s regulated manufacturing network. Own agent backlogs, user discovery, experimentation, adoption, success metrics, governance, responsible AI, monitoring, and lifecycle operations. Partner with engineers, data scientists, manufacturing SMEs, Quality, Cybersecurity, and business stakeholders to convert manufacturing knowledge and user needs into production-grade intelligent agents that improve productivity, decision-making, and operational performance.

Performs biopharmaceutical manufacturing activities in a cGMP-regulated facility, troubleshooting routine issues, supporting deviation investigations, maintaining SOPs and batch records, mentoring colleagues, applying Lean tools, and assisting with facility startup, installation, and validation. The role is fully onsite and operates on rotating 24/7 day and night shifts, with comprehensive training and development provided.

Leads Pfizer’s enterprise applied AI strategy, architecture, governance, operating model, and transformation efforts. Drives portfolio-level technical decisions, reusable capabilities, standards, and measurable business outcomes. Provides hands-on architecture and code review using modern AI and agent frameworks while leading engineers, contractors, and vendors. Oversees quality, security, performance, spending, and technical direction, mentors technical leaders, and evaluates emerging technologies and industry trends.

Lead design, delivery and maintenance of GMP/GDP audit strategy for biologics, aseptic, small molecule and medical device areas. Plan and execute complex audits, coach auditors, analyze regulatory intelligence, drive corrective actions, support inspection readiness, and partner with PGS/PharmSci and site stakeholders to ensure compliance and continuous improvement.

Lead HEOR and evidence strategy for obesity and internal medicine early-pipeline assets. Design and oversee RWD studies, economic models, and patient-reported outcomes; influence trial design; manage evidence generation, publications, vendor relationships, and cross-functional stakeholder engagement to secure reimbursement and patient access.

Lead global HEOR and evidence-generation strategy for obesity assets. Design and execute RWE, economic models, and PRO strategies; create launch dossiers; manage cross-functional teams, vendors, budgets, and external partnerships to support reimbursement and patient access.