Pfizer

ContentManagement

Mexico City, Mexico FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“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.

Problems you'll solve

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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