Analytical Operations and QC Laboratory Senior Technicia - 9 month

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 environment

• Deliver data treatment/elaboration and analytical reports of high quality in a digitally agile manner.
• Interact with customers when needed, with the aim of result discussion or coordination of routine and/or validation activities.
• Works autonomously for the execution of either routine or non-routine activities within established procedures and practices that require knowledge of technical concepts or specialized technical expertise, i.e stability.
• Strong expertise in GMP environment.
• Validate GMP methods including analysis and documentation. Method validation knowledge is mandatory.
• Actively seeks, shares and re-applies knowledge in own field of activities.
• Actively recommends and leads analytical workflow improvement initiatives in a cross functional setting.
• Presents and defends relevant topics during health authority inspections.
• Ability to write GMP documentation: URS, protocols, reports, working instructions, deviations, CAPA, CCP Actions.