Regional Regulatory Submissions Senior Associate

Pfizer; Ciudad de México; Híbrido; MXN 600.000 - 900.000; Jornada completa

Descripción de la vacante

Pfizer is seeking a Senior Associate for the RIO Execution Hub to manage end-to-end regulatory dossiers across multi-regional, regional, and national levels, from initial registrations to product withdrawal. Hybrid work location with emphasis on timely, compliant, and efficient submissions and lifecycle support.

Responsibilities include QA reviews, local document authoring, and collaboration with submission hubs to align with regulatory strategies and launch plans.

Formación

• Bachelor degree in Pharmacy, Life Sciences, Business or Information Technology (desirable).
• Advanced to fluent English; multilingual skills desirable.
• Experience with regulatory, quality or compliance in pharma preferred.

Responsabilidades

• Ensure timely delivery of local M1 dossier components and related regulatory documents.
• Perform quality review/approval of dossier materials and translations as needed.
• Support for HA queries, DHPC responses, and responses to medical information requests.
• Partner with regional and hub teams to meet submission delivery priorities and lifecycle management.

Conocimientos

Regulatory submissions

Quality assurance

Regulatory knowledge

Microsoft Office

Educación

B.S./B.Scs. in Pharmacy/Life Sciences/Business/IT

Herramientas

Microsoft Office

Descripción del empleo

Pfizer is seeking a Senior Associate for the RIO Execution Hub to manage end-to-end regulatory dossiers across multi-regional, regional, and national levels, from initial registrations to product withdrawal. Hybrid work location with emphasis on timely, compliant, and efficient submissions and lifecycle support.

Responsibilities include QA reviews, local document authoring, and collaboration with submission hubs to align with regulatory strategies and launch plans.