Pfizer
ContentManagement
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Content Management at Pfizer. Skills: content management governance, content lifecycle management, content reuse, content performance, content integrity, compliance. Lead content management governance for the EM-C3oE. Act as a subject-matter expert on tagging standards, content taxonomy, and metadata quality”
What You'll Achieve.
faster time-to-market; higher reuse rates; consistent compliance; scaling best practices; operationalizing reuse-led content production; enabling markets to operate high-performing local production cells aligned to regional standards; increasing reuse; standard tagging; adoption of new technologies; content integrity; governance; reuse readiness; operational excellence; content systems thinking; content managed as scalable assets; high levels of reusable local content aligned to regional standards; faster time-to-market; higher reuse and scalable content systems; governance and compliance by content; Enablement of local production cells; Adoption of AI-enabled and next-generation content workflows
Industry & Context.
analytical skills to interpret reuse, performance, and efficiency metrics
What They're Looking For.
Must Have
3 + years of experience in the pharmaceutical industry, Bachelor’s degree in Pharmaceutical Sciences, Health Sciences, Life Sciences, or related field, Fluent English proficiency, written and verbal
Nice to Have
Experience with medical information management and/or scientific publications, Experience with digital or promotional content platforms (e. g. , Workfront, DAMs, content management systems)
What You'll Do.
Lead content management governance for the EM-C3oE
Act as a subject-matter expert on tagging standards
Ensure consistent application of content
and reference standards
Manage the regional promotional content submission and approval process
Monitor approval workflows and proactively identify process optimization opportunities
Support the evolution from content execution to content systems thinking
Track and analyze content timelines
and market consumption
Support the EM-C3oE objective of enabling markets to deliver high levels of reusable local content aligned to regional standards
Provide insights and recommendations to improve reuse adoption
and content performance
Support the identification
and management of scientific and medical information
Collaborate with medical
and operations stakeholders to safeguard content quality and compliance
Actively participate in the day-to-day operational management of the EM-C3oE
Partner closely with the Content Catalyst Lead
and local markets to enable adoption of EM-C3oE best practices
Contribute to the Center of Excellence’s role as a regional reference point and strategic enabler
How You'll Work.
Team & Collaboration
cross-functional coordination; cross-functional, multi-market environment; Collaborate with medical, creative, and operations stakeholders; Partner closely with the Content Catalyst Lead, Account Executive, Brand teams, and local markets
Communication Scope
Fluent English proficiency, written and verbal; Excellent written and verbal communication skills
Process & Methodology
process management, resource planning, operational excellence, process optimization opportunities, cycle time reduction, effort reduction, rework reduction
Full Job Description
Work Location Assignment: Mexico City, Must be able to work from assigned Pfizer office 2-3 days per week, or as needed by the business _**Role Summary**_ The **Content Management** plays a critical role in the **EM Content Catalyst Center of Excellence (EM‑C****3****oE)** by enabling the organization’s mission to **set the standard for content production across Emerging Markets**. This role is accountable for ensuring **content integrity, governance, reuse readiness, and operational excellence** across the end‑to‑end content lifecycle. Acting as a **guardian of content systems, metadata, and scientific accuracy** , supports EM markets in achieving **faster time‑to‑market, higher reuse rates, and consistent compliance**. The role directly contributes to the EM‑C3oE vision of **scaling best practices, operationalizing reuse‑led content production, and enabling EM markets to operate high‑performing local production cells aligned to regional standards** , including increasing reuse, standard tagging, and adoption of new technologies. **** _**Key Responsibilities**_ **Content Governance & Standards Enablement** * Lead **content management governance** for the EM‑C3oE, ensuring alignment with regional standards, Pfizer policies, regulatory requirements, and scientific accuracy. * Act as a **subject‑matter expert on tagging standards, content taxonomy, and metadata quality** , ensuring all content is reusable, searchable, and compliant across EM platforms. * Ensure consistent application of **content, claims, and reference standards** that underpin the EM‑C3oE operating model. **End‑to‑End Content Lifecycle Management** * Manage the **regional promotional content submission and approval process** across Emerging Markets using **Adobe Workfront, GCMA, CANVAS**. * Monitor approval workflows and proactively identify **process optimization opportunities** to reduce cycle time, effort, and rework. * Support the evolution from **content execution to content systems thinking** ,
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