CSV Engineer for Pharma industry

Description: Key Accountabilities: Development, implementation and execution of URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities. Develops, implements and executes validation studies for cGMP-critical computerized systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. Hands-on activity envisaged in relation to this. Generates validation documentation (protocols/reports) and provides assistance with the execution of protocols for computerized systems. Responsible for the va…