Pfizer

Product License Maintenance Manager

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Suba, Bogotá D.C., Distrito Capital, COL

Hybrid

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

Use Your Power for Purpose
We're committed to delivering medicines to the world with greater speed, without compromising on excellence and integrity. Navigating both local and global regulations is crucial, and the dynamic regulatory landscape demands innovative thinking and meticulous attention to detail. Your role will be instrumental in ensuring that our regulatory submissions are prepared, published, tracked, and quality-controlled to meet the highest standards. Your contributions will help us bring life-saving medicines and vaccines to patients around the world more efficiently and effectively.
What You Will Achieve
In this role, you will:

Assist in the preparation, publication, tracking, and quality control of regulatory submissions, ensuring compliance with document management standards.
Coordinate enterprise-wide regulatory management systems, train team members, and develop and implement strategic plans.
Contribute to moderately complex projects, manage your own time to meet targets, and develop plans for short-term work activities.
Execute designated operational tasks through the use of standards and tools, conforming to regulatory submission milestones and obligations.
Support the interpretation of regulatory guidelines to produce business requirements and ensure their implementation at local and regional levels.
Collaborate with team managers to forecast and manage project-specific resources, utilizing flexible resourcing and global load sharing as standard practice.
Act as a Subject Matter Expert in dossier types and processes and handle curriculum and training assignments.

Here Is What You Need (Minimum Requirements)

BA/BS with 2+ years of experience or MBA/MS with any years of experience
Deep understanding of the drug development process, regulatory affairs, and submission management
Familiarity with systems and electronic technologies that support submission and planning activities
Exceptional organizational skills and a keen attention to detail
Ability to present scientific data effectively, both verbally and in writing
Proficiency in English

Bonus Points If You Have (Preferred Requirements)

Master's degree
Familiarity with pharmaceutical organizational structures, systems, and culture
Experience in project management
Strong analytical and problem-solving skills
Ability to work independently and as part of a team
Ability to manage multiple projects and priorities simultaneously
Experience with global regulatory submissions and requirements
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: On Premise
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.
Regulatory Affairs

What the Team is Saying

Pfizer Compensation & Benefits Highlights

Parental & Family Support — U.S. materials describe up to 26 weeks of parental leave (including up to 12 paid non‑medical weeks), with phased return‑to‑work plus fertility, adoption, and surrogacy financial support, backup care, lactation support, and caregiver leave. These offerings indicate depth in family‑building benefits and day‑to‑day caregiver resources.
Healthcare Strength — Core programs commonly include medical, prescription drug, dental, vision, mental‑health/EAP resources, disability insurance, preventive health programs, and free or reduced‑cost vaccinations. Voluntary Benefit Extras and wellness resources broaden coverage and access.
Retirement Support — Career pages and postings note a 401(k) with company matching plus an additional company retirement savings contribution in some plans. Company materials also reference financial‑planning education and colleague‑directed retirement funds.

Learn more about Pfizer's Compensation & Benefits →

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Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

Hybrid

Bogotá, Distrito Capital, COL

121990 Employees

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The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.