Description
ResponsibilitiesProvide for the Computerized System Life Cycle Compliance for validated and non-validated computerized systems, web and mobile applications, and websites.
Review and Approval of SLC Deliverables
Validation Master Plan (creation and updates)
Computerized System Periodic Reviews per the Validation Master Plan
21 CFR Part compliance
Quality Assurance Library activities (physical library maintenance activities.)
SKILLS:
Must have experience in Pharma and with the GxP regulations