On that role, you will ensure compliance with electronic data integrity (e-DI) processes in QC laboratories and Manufacturing. This includes performing QA oversight, reviewing audit trails, approving CSV/Qualification documents for equipment (e.g., HPLC, GC, MES), and defining critical data flows to maintain QA integrity. You will also support KPI maintenance and act as an e-DI expert within the organization. […]
Review and approve e-DI deliverables such as URS, FRA, and qualification reports in alignment with current guidelines.
Approve equipment qualification reports and audit trails according...