- **Labeling/Artwork Systems and Data:** * Support the compilation of data from various sources, generate, and maintain dashboards, business scorecards, and reports.
Influence decision-making through data-driven insights and stakeholder engagement.
* Investigate new technologies that enable better business efficiency, champion system changes, and adoption.
* Work across all necessary stakeholders within and outside GRS to align business needs and expectations to technologies and long-term technology roadmaps.
* Contribute to designing and building system user requirements, reviewing configuration specifications, and resolving system record investigations.
* Contribute as a member of system change control boards and impact resolution teams and lead business discussions regarding specific projects and priorities.
* Lead process development by translating business requirements into current and future business processes.
* Keep informed of industry labeling/artwork trends and evaluate against and for Pfizer best practice.
- **Acquisitions, Collaborations & Divestitures Coordination:** * Serve as the primary point of contact for label exchange activities under Pharmacovigilance Agreements.
* Coordinate timely and compliant exchange of labeling information with external partners.
* Monitor and resolve discrepancies, ensuring alignment with safety and regulatory commitments.
* Lead labeling-related activities during acquisitions and divestitures, including due diligence and integration planning.
* Act as the central liaison between internal teams and external stakeholders to ensure seamless transitions.
* Develop and execute labeling strategies that support business continuity and compliance.
- May support one or more of the pan-portfolio labeling intelligence processes including but not limited to Pfizer Reference Label management across therapeutic areas; Maintenance of the Regulatory Requirements Database for international labeling; Single Reference Safety Document identification and management; Innovator Monitoring for the generic portfolio; North Star; Support audits and inspections by ensuring data readiness and traceability.
* Bachelor's Degree or equivalent with 8 + years relevant experience in global/multi-national pharmaceutical environment, including direct experience either in Labeling or Regulatory Affairs.
* Experience with Business Analytics required.
* Experience in interpreting and applying global and local regulatory guidance around labeling/regulatory and associated supportive documentation desirable.
* Ability to partner with wide range of business stakeholders, crossing multiple divisions across multiple countries/culturesClear and adaptive verbal and written communication skills * Advanced academic qualification/degree desired, equivalent relevant professional experience will be considered.
* Strong problem-solving skills and the ability to develop new options in non-standard situations* Excellent interpersonal skills and the ability to mentor and guide others* Strong facilitation and project management skills* Excellent knowledge of tools used to design processes and process flows, etc.
* Knowledge and experience with labeling or similar tracking systems* Knowledge of XML, regulatory tracking, document management systems, various reporting tools* 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, including risk management and ethical usePfizer careers are like no other.
In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives.
We're looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.
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