Sonas Technical are currently on the lookout for a CQV Engineer for our client, a multi billion global-leading pharmaceutical company. This is a initial 12 month contract and the successful candidate will will work on major €140 million pharma project in Cork. Our client is open to both PAYE and contractors for this role. A market leading remuneration package is available for the successful person.Why apply with Sonas ?We can provide insights to the best salaries, rates and benefits on offerOne point of contact – We can manage all your applications, interviews and negotiationsWe will get your CV seen by the right hiring managersKey Responsibilities:Preparation of documents associated with lifecycle of C&Q activities for a IV, FT, IQ, OQPreparation and execution of FAT, Commissioning and SAT protocolsPreparation and execution of Qualification protocols (IQ and OQ)Design Review (DR) and Design Qualification (DQ) protocol preparation, execution and follow-upField Walkdowns of systems as part of transfer of ownership of the system from ConstructionEnsuring safe operation of the system prior to and during start-up functional testing and Qualification phaseInstallation Verification executionSystem Start-up activitiesFunctional Testing of systemsChange Management activities during project lifecycleSummary Report writingOrganize and review daily tasks/verifications and track the progress of the activities assignedContractors and/or Vendors coordinationInterfacing with representatives on project team, Construction, Engineering, Automation, Quality and End Users during the different project phaseKey Requirements:Relevant 3rd level degree5 year’s experience of C&Q activities in a large project environment within the pharmaceutical or biopharma industries.Delta V experience is advantageous.Hands on expertise required in one or more of the following areas: Upstream/Downstream Process Manufacturing Equipment, Grey/Black Utilities or HAVC.Experience with Regulatory and industry standards for GMP and GEP Tags: