Ensured compliance with regulatory standards, prepared technical dossiers for product registration, monitored legislation, conducted technological surveillance, and updated internal databases.

Managed regulatory compliance for absorbent products in Andean, Caribbean, and South Cone regions. Provided technical support to quality, marketing, and innovation teams.

Formulated and characterized nanocomposites, validated anticaking agents, standardized manufacturing protocols, and performed statistical analysis for process improvement.

Planned and executed >100 trials for sulfur removal, achieving higher than expected results. Developed nanofluids and optimized manufacturing processes.

Evaluated cell viability, cytotoxicity, and genotoxicity. Optimized protocols for ECM decellularization and managed regulatory compliance for medical device materials.

Conducted biocompatibility assessments, developed standardization procedures, and ensured compliance with international standards (ISO, ASTM, FDA).