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 responsibilities
- Review and update the configuration of metadata hierarchies based on current operational requirements
- Validate hierarchies / data flows to ensure they align with industry and internal compliance standards
- Collaborate with internal teams, including IT, Quality Assurance, and Operations to ensure seamless integration of updated hierarchies
- Conduct comprehensive testing and troubleshooting of the updated configurations
- Provide detailed documentation of the updated configurations and validation processes
- Ensure all changes are documented and comply with GxP regulations and other relevant industry standards
Required qualifications and experience
- Experience working with GxP regulations and validation processes within a life sciences or pharmaceutical environment
- Excellent problem-solving skills and the ability to work independently in a fast-paced environment
- Strong communication skills, with the ability to work effectively with cross-functional teams
- Experience with project management, documentation, and reporting
- Experience with data integrity and compliance in regulated industries
Preferred
- Prior experience as a consultant in system validation and configuration in the biotechnology or pharmaceutical sectors
- Understanding of database architecture, data flows, and configuration management within data management systems
