Regulatory Strategy Lead, Mexico City

Pfizer

Ciudad de México

Hybrid

MXN 1,800,000 - 2,400,000

Full time

40 hours ago
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Benefits offered by this job

Hybrid work model

Job summary

Pfizer in Mexico City is seeking a Regulatory Manager Team Lead to guide the regulatory team across markets. You will shape regulatory strategy, lead cross-functional product teams, and manage MA applications while coordinating with above-country hubs to align local and regional plans.

The role requires strong leadership, fluent English and Spanish, and proven experience in regulatory affairs for human medicinal products. Hybrid office-based role in Mexico City.

Qualifications

  • Life sciences or chemistry degree required; honours level or equivalent.
  • Masters or PhD in regulatory science preferred.
  • Previous regulatory experience in Human Medicinal Products is essential.
  • Strong leadership, coaching and mentoring abilities.
  • Excellent written and verbal communication; fluent in English and Spanish.

Responsibilities

  • Lead and oversee the regulatory team and provide strategic input across markets.
  • Drive regulatory submissions strategy and interaction with NRAs and authorities.
  • Coordinate projects within the cluster and with above-country hubs.
  • Ensure compliance with Pfizer standards and regulatory requirements.
  • Develop and implement regulatory plans aligned with business goals.

Skills

Regulatory strategy
Team leadership
Cross-functional
Regulatory submissions
English & Spanish
Analytical thinking
Project management
Communication

Education

Life sciences or chemistry (Honours)
Masters/PhD in regulatory science (preferred)

Job description

Pfizer in Mexico City is seeking a Regulatory Manager Team Lead to guide the regulatory team across markets. You will shape regulatory strategy, lead cross-functional product teams, and manage MA applications while coordinating with above-country hubs to align local and regional plans.

The role requires strong leadership, fluent English and Spanish, and proven experience in regulatory affairs for human medicinal products. Hybrid office-based role in Mexico City.

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