José Luis López Escandón in

José Luis López Escandón

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Associate Director Regulatory Affairs at MSD
📍 Mexico City Metropolitan Area

José Luis is the Associate Director of Regulatory Affairs at MSD in Mexico, leveraging over a decade of experience in the pharmaceutical sector. His background includes quality assurance and control roles at Bristol Myers Squibb and Bausch + Lomb. He holds a Masters from the Universitat de Barcelona.

Beyond his formal role, José Luis shows a deep passion for the history and scientific milestones of public health. He is interested in the evolution of medicine, particularly the development and rigorous regulatory processes that bring new vaccines and treatments to the public, ensuring their safety and efficacy.

He has a keen interest in the historical context of medicine, such as the development of the first vaccine in 1796.

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Experience
20 Years
Current Role
Associate Director Regulatory Affairs
Job Level
Mid-senior
Location
Mexico City Metropolitan Area
Personality Overview

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Decision Approach
Work Preference

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Priorities

Topics José cares about

Pharmaceutical Regulation
His entire career is focused on regulatory affairs and quality assurance, with specific expertise in COFEPRIS regulations for Mexico and the Caribbean.
Vaccine Development
Shares content on the challenges of vaccine approval and the history of vaccine development, indicating a strong professional and personal interest.
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Career

Work history

5-2021
Associate Director Regulatory Affairs
MSD
8-2014 - 4-2021
Senior Regulatory Affairs Specialist
MSD
10-2012 - 4-2013
Especialista en Garantía de Calidad
Kern Pharma
2-2011 - 7-2012
Quality Assurance Lead
Bausch + Lomb
2-2003 - 7-2010
Quality Control Supervisor
Bristol Myers Squibb
In the press

Media appearances

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Education
2012 - 2014
Master en Gestión Empresarial en Industria Farmacéutica y Afines.
Universitat de Barcelona
2007 - 2008
Especialista
Universidad La Salle, A.C.
Social presence
in
Behavioral profile

DISC profile (public)

DISC behavioral profile

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