Company: Pfizer
Location: Marlow
Posted: April 10th, 2026
We are committed to bringing medicines to the world at a faster pace without compromising on excellence and integrity. Navigating the ever-changing regulatory environment compliantly requires forward-thinking and meticulous attention to detail. Your dedication and expertise are vital in expanding and accelerating patient access to Pfizer medicines and vaccines.
In this role, you will be responsible for:
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.
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.
Maintain the integrity and accuracy of the labeling and artwork pan-portfolio intelligence data across applicable business and regulatory systems.
Ensure proper data governance, version control, and metadata management.
Coordinate the labeling universe maintenance process, including analysis and tracking of updates. Ensure regular data quality checks are performed and support the resolution of identified issues.
Ensure correct label tracking strategies are implemented in the setup of new products, updated during the lifecycle of the product and the correct end of label maintenance activities are performed.
May support one or more of the pan-portfolio labeling intelligence processes including but not limited to:
Provide strategic and operational support for high-impact, cross-portfolio initiatives.
Lead or contribute to special projects that enhance labeling processes, systems, or compliance.
Collaborate with global teams to drive innovation and continuous improvement.
Provide project management support across labeling initiatives, ensuring timelines, resources, and deliverables are met.
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 with interacting autonomously with leaders and working in a matrix team environment a must.
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/cultures.
Proven leadership driving highly complex projects to meet evolving business needs.
Ability to manipulate and understand complex data.
Mastery of processes, tools and techniques for planning and monitoring multiple complex projects to established deadlines.
Clear 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 use.
Work Location Assignment: Hybrid
Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.
One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.
We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.
We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!
Regulatory Affairs
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