Senior Cqv Engineer - Biotech

Job DescriptionOur client is an international engineering and PM consultancy with Life Science projects across Ireland.The C&Q Engineer shall be responsible for carrying out the following project related activities:Preparation of documents associated with lifecycle of C&Q activities for a IV, FT, IQ, OQ.Preparation 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 phases Installation Verification executionSystem Startup 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 phases.RequirementsA degree in science or engineering or equivalent.
Or A certificate/diploma in similar areas with appropriate industrial experienceMinimum of 5 years experience of C&Q activities in a large project environment within the pharmaceutical or biotech industries.Hands on expertise required in one or more of the following areas: API Facilities, Grey Utilities, HVACExperience with Regulatory and industry standards for GMP and GEPSelf starter & good team playerGood oral & written communication skillsPackageHourly rate of €65 - €75 per hour