The incumbent will be a part of the IT Computerized System Validation (CSV) Department and will perform and/or direct GxP computerized system validation projects in compliance with cGMP, 21 CFR Part 11 and Annex 11. This individual will ensure that GxP systems meet intended uses and comply with applicable regulations, current industry practices, and Revance’s policies and procedures. Validation projects may include manufacturing systems, lab systems, facilities systems and steady state activities around these applications.
Bachelor's degree in Engineering, Science or related technological field
Bachelor’s degree in Pharmaceutical Science, Biomedical Engineering, or Management of Information Systems (MIS).
Knowledge, Skills and Abilities
Risk Management Tools, MS Word, Excel, PowerPoint, Visio, Project and Outlook
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