Jefferson Wells * Wavre * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Contracting – Brabant Wallon - Vos responsabilités * Writing, reviewing and approving of validation plans and validation summary reports * Reviewing and approving of design documentation (TCD, ERES, URS, DQ, ...) * Reviewing and approving of qualification protocols and reports (IQOQ & PQ) * Writing and reviewing of Periodic Review Reports (PR) * Reviewing and approving of CSV specific documentation (inventory, ...) * Reviewing of CVS specific SOP'S and Templates * Ensure the proper execution of the qualification and validation activities with respect of the GSK validation methodology to maintain the validated status of automated and computerized systems. * Ensure QA activities on quality systems (CAPA, Deviation, Change Control, ...) related to automated and computerized systems.
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