**Job Summary**

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...