US_East | Desktop Support_L3

Description:Possible 3 Month CTH | No Fees | Do Not Re-Post| Confidential R2D2 9506997 Role R&D Regulatory submission systems Work location King Of Prussia,PA (Remote) Rates as follows: $ 78 hr/AI Background Check: MANDATORY R&D Regulatory submission systems: R&D Regulatory submission systems Location: KOP (King Of Prussia) / Remote Role Description: • L2/L3 Support: Service requests, incident resolution, release management, minor enhancement on list of regulatory submission applications. • Performing Computer System Validation activities and authoring documents for regulatory submission systems in the Biotech/Pharmaceutical Industry Skills Requirements: • The person must come from IT Departments (R&D IT support) from Pharma or/and Biotech industries and should have ITIL knowledge (Incident/Change/Knowledge/Problem Management). • Some knowledge of and experience in Regulatory Information Management System Administration, Regulatory Submission Process and Regulatory Affairs business processes workflows involved in interaction with Health Authorities i.e FDA. And EMA. • Technical skills: Windows Server, Documentum, DQL/SQL • Knowledge of following regulatory submission applications preferred: • Lorenz Docubridge • InSight for Publishing/Viewing • Veeva Vault RIMS (Regulatory information Management System) Key Words (for sourcing): • Pharma or/and Biotech, Regulatory Affairs • Regulatory Submissions **VIDEO INTERVIEW IS MANDATORY -ERM - Miguelangel Buonafina | Capgemini |North America Tel.: +1 888-229-2961 Ext 13578

Created: 2026-04-02