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 requiredExecute, under supervision, equipment qualification and requalification for manufacturingParticipates in the operation of process equipment as well as associated documentationSupport execution of preventative maintenance of pharmaceutical process equipment and utilitiesSupports equipment readiness to support the production schedule and is in proper condition/calibrationProvide operational coverage for manufacturing equipment and utilitiesSupport production personnel on equipment and utility operationSupport ...