Position: Validation leadContract: 06 months with possible extensionLocation: 1300 Wavre, Belgium (Onsite)Language: French is MustJob Description:Prepare Validation Plan and Validation ReportEnsure documents are administered and managed in accordance with this Validation Plan and the governing Document Management Plan (3)Ensure that the system is validated and used in a compliant manner, if system is deemed GxP. Ensure that appropriate user procedures are in place.Knowledge on GxP and supporting pharma customersKnowledge in performing Risk AssessmentsMonitor and assist validation and release related progress of the project through to closurePrepare, review and approve project deliverables in accordance with validation PlanEnsure that appropriate support and maintenance procedures are in place prior to the production releaseUnderstanding of Smart control assessment and QA concepts. Previous experience and familiarity with smart controls will be a plus.Work with tech/app owners to guide and assist in QA and compliance related aspects of the apps transition.May also need to help in testing area to some extent.French speaking.Should work from GSK House