About this opportunity
Redolent, Inc lists this US_East | Desktop Support_L3 opportunity in king of prussia, Pennsylvania. Review the employer’s description below for duties, qualifications and application requirements.
Job description
R2D Role
R&D Regulatory submission systems
Work location: King Of Prussia, PA (Remote)
Rates as follows: $78/hr
Background Check: MANDATORY
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.
Worksite address
king of prussia, PA, 19406, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.