Summary
Candidate must have knowledge of GMP requirements and experience in a pharmaceutical manufacturing environment.
• Analyzes business procedures and data maps and ensure data can be entered accurately to target system.
• Confers with personnel of organizational units involved to ascertain specific output requirements key metrics, such as data counts, data status and accuracy of data migrated for management reports.
• Attends specification meeting with project team workers to determine scope and limitations of project, issues encountered and need for escalation.
• Reviews data migration workflows to understand tasks needed to successfully migrate data to target system.
Reviews GxP and quality data procedures in data base management system for planning and implementing data migration activities
• Conducts quality reviews of data migrated. Investigates, documents and reports data anomalies associated with the quality, accuracy and completeness of data migrated to target system.
• Plans and prepares technical reports, memoranda, and instructional manuals relative to the establishment and functioning of complete operational systems.
Other important characteristics:
• Demonstrated strong attention to detail as Candidate must be able to manage significant detail for this data entry project.
• Strong communication skills both verbally and in writing.
• Is action and results driven as this project will have aggressive timelines.
• Knowledge of both TrackWise and Veeva? If not, ability to grasp new systems quickly to ensure they can enter data from one system to another.