Use Your Power for Purpose

Our mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, or exploring ways to bridge data gaps, your role is vital. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.

What You Will Achieve

In this role, you will:

Monitor and manage the company's drug, biologics, and medical devices surveillance program, ensuring comprehensive oversight.

Intake, evaluate, and process adverse reports for both clinical trials and post-marketing activities, ensuring accurate and timely handling.

Act as a subject matter expert, liaising with key partners regarding safety data collection, reconciliation, and ensuring regulatory compliance.

Review, analyze, prepare, and complete safety-related reports to determine the safety profile of products and meet regulatory requirements.

Verify the accuracy, consistency, and compliance of processed cases, and review case data for special scenarios, ensuring high standards are maintained.

Manage safety resources within the local team, provide specific pharmacovigilance or product knowledge, mentor colleagues, and maintain advanced knowledge of Pfizer's product portfolio and corporate policies.

Here Is What You Need (Minimum Requirements)

BA/BS with at least 2 years of experience or MBA/MS with any years of experience

Strong organizational and project management skills

Solid knowledge of global regulations and guidelines for drug development

Demonstrated analytical and statistical skills

Fluency in spoken and written English

Bonus Points If You Have (Preferred Requirements)

Master's degree

Relevant pharmaceutical industry experience

Familiarity with management of performance metrics

Strong problem-solving skills

Proficiency in safety database and data mart search functions

Extensive knowledge of Mexican legislation (NOM-220, NOM-240, and good pharmacovigilance practices).

Other Job Details:

Last Date to Apply for Job: Oct 23rd, 2025.

Work Location Assignment: Mexito City, Mexico. Must be able to work from assigned Pfizer office 2-3 days per week, or as needed by the business

EEO (Equal Employment Opportunity) & Employment Eligibility 

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.