Development, qualification, and transfer of analytical methods for biopharmaceuticals (RP, SEC, IEX, NP, HIC, CE, icIEF)Troubleshooting chromatographic- and electrophoretic- related problemsDevelopment of automated sample preparation on Vantage VoV platform. Writing, validation and optimisation of scripts to support PhysChem group needs.Continuous improvement of existing methods and processes. Implementation of new technologiesPerforming diverse analytical tests, evaluating results, and presenting results to the CMC TeamEnsure work is performed in accordance with appropriate safety and quality regulations. Supporting the CLD, USP, and DSP analytical activities according to plan and timelinesProviding analytical expertise to various levels of CMC projectsAuthoring/reviewing analytical documents such as protocols, reports, SOPsManage inventory and maintenance of reagents/consumables and laboratory equipment.Training of new comers (technicians, scientist)

Analysis of pharmaceutical formulations by capillary electrophoresisDevelopment and validation of analytical methods for the detection of falsified drugs.

Physico-chemical analysis of pharmaceutical formulationsMicrobiological controls of formulations and production zones Developments and validations of quantitative and qualitative analysis methods (UHPLC-MS/MS, LC-UV, CE-UV) Installation and programming of a sample preparation robot for toxic samplesStability studies of pharmaceutical formulations Design of a secure laboratory for the handling of toxic agents (www.cytoxlab.ch) Management of the laboratory & instruments

Headteacher - IT maintenance - Creation of an Integrated Library SystemCreation of a learning resources center: I was responsible for the creation and development of a library management system. This PHP/SQL based system enables students to carry out documentary researches. The software is also used to track items owned, orders made, and documents borrowed by students.

Master Thesis : Research and Development of new Odorant Molecules for PerfumerySynthesis and identification of molecules using various reactions and analysis methods (GC, HPLC, MS, NMR ¹H and ¹³C). Use of purification processes (flash chromatography, Fischer distillation) to ensure the high quality of the delivered products. Research of existing literature and study of patentability criteria to confirm that the newly synthesized molecules could be protected by a patent.

Project on total synthesis of natural products. Participation in Jerantinine E total synthesis project.

Quality Control - Food and pharmaceutical microbiological testing - Sample reception - Laboratory management - Media preparation and fertility control - Metrology of laboratory equipment.