Jobs at Pfizer

Executes global CMC regulatory strategies for post-approval pharmaceutical changes, including product change assessments, health authority responses, regulatory submissions, dossier updates, and technical justifications. Coordinates cross-functional reviews, document sign-off, query and commitment management, risk escalation, and regulatory system maintenance. The role requires applying international regulatory guidelines and managing multiple projects under team-lead guidance.

Supports global pharmaceutical regulatory CMC activities for license renewals and annual reports. Authors and compiles CMC dossier contributions, reviews post-approval changes and stability information, applies regulatory guidelines, develops technical justifications, coordinates document reviews, manages commitments and queries, and updates submission components. Collaborates with global regulatory strategists, manufacturing, supply, and cross-functional teams while monitoring timelines, risks, compliance, and submission accuracy.

Supports CMC regulatory activities for pharmaceutical license renewals and annual reports across global markets. Responsibilities include authoring and compiling regulatory dossier contributions, reviewing technical and stability information, applying U.S. regulatory guidelines, coordinating document reviews and approvals, updating dossier components, managing timelines and risks, and using Pfizer regulatory systems. Requires postgraduate education in Pharmacy or Science and foundational knowledge of post-approval regulatory requirements.

Leads global logistics data governance, accuracy, stewardship, and data quality initiatives. Manages Data Operations analysts, develops data strategy and quality metrics, validates data models, and supports planning and analytics. Partners with digital, supply chain, manufacturing, finance, logistics, and external freight-forwarding teams in a global matrix. Oversees recruitment, coaching, change adoption, project alignment, IMEX standards, and continuous improvement across transactional, planning, and master data.

Owns the vision, roadmap, delivery, adoption, and value metrics for AI products across Pfizer’s international commercial portfolio. Translates business priorities into technical backlogs and acceptance criteria, coordinates agile delivery, UAT, releases, vendors, and production handoffs, and guides solutions from prototypes to enterprise-grade systems. The role also supports AI prototyping, stakeholder alignment, user engagement, documentation, and integration across data, platform, security, and commercial teams.

Owns business administration and continuous improvement of Veeva Vault eQMS within a regulated pharmaceutical quality organization. Responsibilities include access management, release coordination, reporting, documentation, configuration advisory, enhancement prioritization, data operations, stakeholder communications, and cross-functional program execution. The role also evaluates AI, automation, and digital transformation opportunities while ensuring GxP compliance, data integrity, system continuity, and effective quality operations.

Lead the delivery of AI products across international markets by coordinating internal engineers, contractors, and vendors. Establish engineering standards, make technical decisions, review code, ensure testing and release readiness, and guide solutions from proof of concept through enterprise production. Oversee data, AI, generative AI, agentic AI, and full-stack applications while managing dependencies, technical debt, and delivery quality. Collaborate with product, engineering, data science, security, and global stakeholders, and evaluate emerging technologies.

Designs, develops, and maintains high-quality clinical databases for pharmaceutical studies. Builds data capture solutions, ensures clinical data integrity, applies database and data standards, and supports study-specific data review and reporting requirements. Collaborates with cross-functional study teams, follows applicable SOPs, and develops expertise in clinical data capture technologies, relational database programming, drug development processes, regulatory requirements, and CDISC standards.

Develops and executes global medical communications content for vaccines, including manuscripts, abstracts, congress materials, literature reviews, slide decks, educational resources, and multimedia. The role researches and interprets scientific data, ensures accuracy and compliance, coordinates cross-functional stakeholders, manages project timelines, supports training, and adopts generative AI and other content-development tools. Requires advanced scientific education, pharmaceutical medical-content writing experience, strong project leadership, statistical understanding, and excellent communication skills.