Regulatory Affairs Professional This role is responsible for ensuring regulatory compliance across South America, supporting product registrations, renewals, and post-marketing maintenance. The ideal candidate will have a strong understanding of regional regulations, including INVIMA, ANVISA, DIGEMID, and ISP. The Regulatory Affairs Specialist will be tasked with preparing and submitting regulatory dossiers, monitoring regulatory requirements, and collaborating with internal stakeholders to ensure alignment with business objectives. Additionally, the role will involve supporting product claims validation, labeling compliance, and implementing digital tools to streamline documentation and submissions. To excel in this position, candidates should possess a Bachelor's degree in Chemical Engineering, Pharmaceutical Chemistry, or a related scientific discipline. A minimum of 2 years of experience in Regulatory Affairs is required, preferably within the cosmetics, personal care, pharmaceutical, or consumer goods industries. Strong knowledge of international regulations and proficiency in Microsoft Office Suite are also essential. Your Background - Bachelor's degree in Chemical Engineering, Pharmaceutical Chemistry, or a related scientific discipline. - 2+ years of experience in Regulatory Affairs, ideally within cosmetics, personal care, pharmaceutical, or consumer goods industries. - Strong knowledge of regulatory environments across South American countries, including but not limited to Colombia (e.g., INVIMA), Brazil (e.g., ANVISA), and others. - Familiarity with international regulations is an advantage. - Intermediate to advanced English – must be able to hold conversations and communicate clearly in both verbal and written form. - Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint); knowledge of digital tools and AI technologies for process optimization is a plus. - Detail-oriented, organized, and capable of managing multiple priorities in a dynamic, multicultural environment. - Experience in regulatory submissions using electronic systems or platforms. - Interest or experience in digital transformation, AI tools, or process automation for regulatory tasks.