Configuring System using Studio designer  at form/work level/notifications
Working with the technical team for integration with the different application
create Design specs based on the customization
create validation documents like PQ/IQ
Conduct classroom training for end clients
Build and Promote customization to QA and PROD environments

Optimum Skills or Background
1-3 years of experience in services in a technical/configuration field.
Experience with the implementation of Quality Management systems ( Track wise/ Master control / ETQ/ CEBOS)
Experience in Crystal reporting / Tibco Spotfire
Familiarity with ISO 9000, cGMP and FDA Regulations
Experience with the implementation of MRP systems and Manufacturing Concepts
Strong writing and communication skills
Proficient problem solving ability
Strong Manufacturing or Business process knowledge
Experience in programming concepts

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com