
Analytical chemist with a master's degree in chemistry and extensive experience in pharmaceutical quality control and scientific analysis. Skilled in chromatography, mass spectrometry, and compliance with cGMP/GLP standards. Expertise in method-based assays, impurity profiling, and instrument calibration. Seeking opportunities in chemical analysis and quality control within pharmaceutical laboratories.
• Optimised Synthesis Description: Conducted a multi-step synthesis of a novel ligand for MRI contrast agents, resulting in a high-quality product under expert supervision.
• Streamlined Analytical Processes: Utilised HPLC and LC-MS for reaction monitoring and product purification, ensuring accurate structure confirmation through NMR.
• Enhanced Reporting Techniques: Compiled comprehensive findings and compared results with related ligands, achieving the highest thesis grade.
• Determined ligand protonation constants and the stability of the Mn(II) complex via pH-potentiometric titration.
• Conducted quantitative and potency analysis of compounds in accordance with cGMP and GLP requirements.
• Performed potency testing via UV-Vis spectrophotometry and determined water content using Karl Fischer titration.
• Utilized HPLC for assay determination, optical purity analysis, and impurity profiling.
• Identified and quantified impurities using GC-MS to support product safety assessments.
• Adhered to SOPs, performed instrument setup, and prepared samples with precision.
• Operated an Agilent CE 7100 system with UV detection coupled to a Bruker MaXis II ESI-QTOF mass spectrometer for the analysis of biological and protein samples.
• Verified molecular formulas of compounds based on accurate mass, isotopic patterns, and [M+H]+ / [M+Na]+ adducts, and determined mass accuracy (ppm error).
• Investigation of bottom-up and top-down proteomics workflows, peptide fragmentation (b/y ions), and data analysis using Bruker Compass DataAnalysis under Professor Attila Gáspár.