We are seeking a entry to mid level consultant to assist in updating the metadata and re-validating Data Warehouse data flows to ensure compliance with system requirements and industry (GxP) standards. The ideal candidate will have experience in configuration of data management tools and IT validation processes. Key responsibilitiesReview and update the configuration of metadata hierarchies based on current operational requirementsValidate hierarchies / data flows to ensure they align with industry and internal compliance standardsCollaborate with internal teams, including IT, Quality Assurance, and Operations to ensure seamless integration of updated hierarchiesConduct comprehensive testing and troubleshooting of the updated configurationsProvide detailed documentation of the updated configurations and validation processesEnsure all changes are documented and comply with GxP regulations and other relevant industry standards Required qualifications and experienceExperience working with GxP regulations and validation processes within a life sciences or pharmaceutical environmentExcellent problem-solving skills and the ability to work independently in a fast-paced environmentStrong communication skills, with the ability to work effectively with cross-functional teamsExperience with project management, documentation, and reportingExperience with data integrity and compliance in regulated industries PreferredPrior experience as a consultant in system validation and configuration in the biotechnology or pharmaceutical sectorsUnderstanding of database architecture, data flows, and configuration management within data management systems