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; validate GMP methods including analysis and documentation (mandatory).
Actively seek, share, and re-apply knowledge in your field.
Recommend and lead analytical workflow improvements in a cross-functional setting.
Present and defend relevant topics during health authority inspections.
Ability to write GMP documentation: URS, protocols, reports, instructions, deviations, CAPA, CCP Actions.
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