Join a fast-growing Bioplant in Yverdon-les-Bains during a pivotal expansion phase. We are seeking a QA QC Expert to ensure the highest quality standards for our Drug Substances and Raw Materials.ResponsibilitiesBatch Disposition: Collect and review all records for Drug Substance (DS) and Drug Product (DP) release; chair weekly disposition meetings.QA Oversight of QC: Provide day-to-day quality guidance to the lab, approving specifications, analytical
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;
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