Roles and responsibilities: Experience in Pharma or Med device. Previous experience as a CQV Engineer in the Pharmaceutical or Med Device production environment, to include. Performing Risk Assessments by assessing machinery for potential failure modes/quality issues and then writing reports and procedures. Commissioning and qualifying automated manufacturing equipment. Knowing what a human machine interface is, what a PLC controlled system looks like, how an operator would log into a machine to use it. Investigation of deviations and CAPAs.