Support regulatory activities to ensure products (medicines, medical devices, cosmetics, and nutritional supplements) meet all compliance requirements across assigned markets.
Review and approve promotional materials in line with corporate policies and current regulatory legislation.
Maintain and update regulatory information in systems such as SAP and Veeva Regulatory with high business impact.
Support the preparation and submission of regulatory dossiers, applications, and documentation for new product launches and lifecycle management.
Monitor and assess regulatory changes, ensuring timely adaptation and communication of risks or impacts to stakeholders.
Collaborate with cross-functional teams including Marketing, Supply Chain, Quality, and Logistics to support business initiatives and ensure compliance.
Analyze regulatory issues and contribute to mitigation plans aligned with business needs and regulatory requirements.
Support labeling processes and ensure product claims, advertising, and promotion remain compliant and competitive.
Maintain strong relationships with internal and external stakeholders, including regulatory authorities where required.
Contribute to continuous improvement initiatives and regulatory strategy development within the assigned scope.
Why you?
Requirements
We are looking for professionals with the required skills to achieve our goals:
Bachelor's degree in Pharmacy (required by local regulations).
1-2 years of experience in Regulatory Affairs or similar roles.
Knowledge of regional regulatory frameworks for pharmaceuticals, medical devices, cosmetics, or nutritional supplements.
Experience working with regulatory systems (e.g., SAP, Veeva, or similar).
Intermediate to advanced English proficiency (written and spoken).
Strong communication, stakeholder management, and analytical skills.
Ability to work collaboratively, drive improvements, and manage multiple priorities effectively.
If you feel this is your next career step, apply!
Job Posting End Date
2026-06-19
Equal Opportunities
The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.
Adjustment or Accommodations Request
Note to candidates
The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you r
Benefits
Health insurance
Additional Information
Welcome to Haleon. We're a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we've grown, evolved and are now entering an exciting new chapter - one filled with bold ambitions and enormous opportunity.
Our trusted portfolio of brands - including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® - lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.
Now it's time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose - to deliver better everyday health with humanity - at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.
As a Regulatory Affairs Analyst , you will play a key role in ensuring that products across the LATAM Export Cluster markets comply with all applicable regulatory requirements while supporting commercial objectives. This role involves working closely with cross-functional stakeholders, maintaining regulatory systems, and contributing to regulatory strategies to enable efficient and compliant product launches and lifecycle management.
Gsknch · - Cartago - Tres Rios, Costa Rica