Juan Pablo Ruiz Moreno

Optimized efficiency, accuracy, and traceability of analytical results to meet quality control standards. Developed, optimized, and validated analytical methods, focusing on HPLC-MS techniques. Provided analytical support for API production and small molecule synthesis. Prepared customized reports for data-driven decisions. Maintained and calibrated key instruments such as HPLC, GC, and MS. Authored and updated SOPs to ensure consistency and traceability.

• Conducted analysis of pharmaceutical products under natural, accelerated, and ongoing stability studies, ensuring compliance with regulatory standards. • Determined active ingredient content and dissolution, as well as quantified organic impurities using HPLC, U-HPLC, and GC techniques. • Applied and interpreted official pharmacopoeias to guarantee accuracy and reliability of results. • Prepared, analyzed, and reviewed laboratory reports to support product stability assessment.

- Member of the applied analytical chemistry group (QANAP) - Master Thesis: Analysis of pharmaceutical products in the marine environment: biota. Development and validation of an analytical method for the identification and quantification of pharmaceutical compounds in biological samples of the fish mullus babartus using HPLC-MS and using QuEChERS as an extraction method, within the framework of the European project PHARMASEA.