Validation Engineer II is expected to execute validation and qualification activities for pharmaceutical manufacturing systems in compliance with cGMP requirements, industry standards, and standard operating procedures under guidance from Manager.
**Area Of Responsibility**
+ Supports the execution of equipment validation and maintenance as required + Execute, under supervision, equipment qualification and requalification for manufacturing + Participates in the operation of process equipment as well as associated documentation + Support execution of preventative maintenance of pharmaceutical process equipment and utilities + Supports equipment readiness to support the production schedule and is in proper condition/calibration + Provide operational coverage for manufacturing equipment and utilities + Support production personnel on equipment and utility operation + Support re-qualification of process equipment, testing & ce...