Tayebeh Gorji

- Technical Assistant and R&D Manager Supervision of R&D team for the formulation of new products and scale-up Control of provided pharmaceutical documents according to GMP for obtaining licenses from the Iran Food and Drug Administration Manufacturing set-up

- R&D Supervisor Formulating pharmaceutical capsules, tablets, solutions, and gel products. - Head of R&D department Formulation of different pharmaceutical dosage forms Provide pharmaceutical documents according to GMP

QC Expert • In situ injection monitoring of industrially produced batches Regulatory scientist • Studying scientific and legal documents • Gathering, evaluating, organizing, managing, and collecting information in various forms. • Writing comprehensible, user-friendly, clear product information leaflets and labels. • Preparing documentation like CTD and DMF to present to Iran Food and Drug Administration

Quality control of food and drug products via HPLC-FID, HPLC-Fluorescence, GC, UV-Vis according to ISIRI (Institute of Standards and Industrial Research of Iran) and USP

Thesis Title: Loperamide detection in plasma and urine via dispersive liquid-liquid microextraction (DLLM) combined with solid-phase extraction (SPE).