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
Job Summary
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.
Collaborating with cross-functional stakeholders (Quality, Medical Affairs, Marketing, Manufacturing, and Global Regulatory teams) to ensure timely and compliant product submissions, renewals, and variations.
Exposure to a diverse pharmaceutical and medical device portfolio within a global organization and opportunity to contribute to regulatory strategies that directly impact patient access to innovative eye care solutions.
Matching Summary
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.
Skills & Requirements
Must-have
Mexican regulatory framework knowledge
Product registration processes
GxP standards adherence
Cross-functional collaboration
Nice-to-have
Strong analytical mindset
Resilience and commitment to quality
Dynamic, fast-paced environment adaptability
Key Requirements
Bachelor’s degree in Medical-Biological Sciences, Chemistry, Pharmacy, Pharmacology, or related field