Alcon

Sr. Associate I, Regulatory Affairs Strategy

Ciudad de Mexico, Mexico Full time

Sr. Associate I, Regulatory Affairs Strategy
Mexico City, On-site
 

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.
 

Role Overview

As a Sr. Associate I, Regulatory Affairs Strategy, supporting the Quality & Regulatory Affairs team, you will be trusted to support regulatory strategy, submissions, and compliance activities for Mexico, ensuring our pharmaceutical and medical device portfolio meets local regulatory requirements.

In this role, a typical day will include:

  • Collaborating with cross-functional stakeholders (Quality, Medical Affairs, Marketing, Manufacturing, and Global Regulatory teams) to ensure timely and compliant product submissions, renewals, and variations

  • Coordinating regulatory submissions with plants, agents, and regulatory authorities in Mexico, ensuring accuracy and adherence to timelines

  • Supporting regulatory strategies for new product introductions and lifecycle management activities

  • Reviewing and approving promotional materials to ensure compliance with applicable laws, codes, and ethical standards

  • Ensuring adherence to GxP standards, maintaining accurate documentation, and supporting continuous improvement initiatives
     

WHAT YOU’LL BRING TO ALCON

  • Bachelor’s degree in Medical-Biological Sciences, Chemistry, Pharmacy, Pharmacology, or related field

  • Experience in Regulatory Affairs within pharmaceutical and/or medical device industries

  • Knowledge of Mexican regulatory framework and product registration processes

  • Understanding of pharmacovigilance processes

  • Intermediate English (oral and written), with ability to interact with global stakeholders

  • Strong analytical mindset and attention to detail

  • Ability to manage multiple priorities in a dynamic, fast-paced environment

  • High level of organization, resilience, and commitment to quality and compliance
     

HOW YOU CAN THRIVE AT ALCON

  • Exposure to a diverse pharmaceutical and medical device portfolio within a global organization

  • Opportunity to contribute to regulatory strategies that directly impact patient access to innovative eye care solutions

  • Collaborative leadership environment with autonomy, accountability, and strong cross-functional partnership

     

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Alcon is an Equal Opportunity Employer and takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status.