Your key responsibilities in this role are:Conduct routine analytical testing, method qualification execution as well as stability in an independent manner on:Liquid chromatography (PA, SEC, RP,…)Capillary Electrophoresis (icIEF, CGE-SDS)Able to validate/qualify analytical methods (LC, CE especially, but knowledge of OD, LC-MS, ELISA can be an asset)in GMP environmentDeliver data treatment/elaboration and analytical reports of
YOUR ROLEWithin the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "DSP Manufacturing Senior Technician " who will support the DSP large-scale operations (GMP and pilot).You will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells.You will support the DSP activities from an operational and documentation point of view:
Independently conduct routine analytical testing, method qualification, and stability in a GMP environment in icIEF and/or CGE-SDS)Deliver high-quality data treatment and analytical reports in a digitally agile manner.Interact with customers to discuss results or coordinate routine and validation activities.Work autonomously on routine/non-routine activities requiring specialized technical expertise (e.g., stability).Strong expertise in GMP environment;