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Senior Cqv Engineer For Clean Utilities

Details of the offer

Are you a senior CQV Engineer with 10+ years of experience in commissioning and qualification activities for pharmaceutical facilities and have previous experience as manager/leader of C&Q team?If you have the relevant experience, please forward your CV to ****** for review or call 353 1 7978720 to discuss in confidence.Senior CQV Engineer for Clean Utilities – execution phase - Pharma- Ireland Job Description Our client is an international engineering and PM consultancy with Life Science projects across Ireland.Manage team of C&Q Engineers on high profile client site throughout the project lifecycle.Strong experience with Validation Master Plan, Commissioning Master Plan, project procedures and commissioning and qualification protocols (SAT/Commissioning, IQ and OQ)Design Review (DR) process and GMP Risk Assessment (FMEA) experienceIdentify the appropriate Commissioning and Qualification strategy to apply on specific project and define the list of activities requiredReview and follow-up technical documentation from the early design phase in order to ensure alignment with GMP and CQV requirementsInvestigate and resolve technical issues with assistance from engineers and/or suppliersEnsure site project execution is undertaken in compliance with company guideline, department procedures and safety standardsBe familiar with the Mechanical Completion procedure and Construction scope of work (Walkdown, system acceptance, punch list and follow up)Schedule preparation and progress reviewOrganize and review daily activities of other CQV Engineers assigned to the projectProject management principles to coordinate CQV activities and reporting to internal and Clients PMContractors and Vendors management and coordinationFinal Handover reports to the Client usersThe Senior CQV Engineer reports to the department manager / site commissioning manager and is accountable to coordinate CQV resources, deliverables and activities from the validation approach definition, design review, turn-over systems definition and C&Q activities at site.Requirements Degree or equivalent in an engineering related discipline10+ years of experience in commissioning and qualification activities for pharmaceutical facilitiesStrong leadership and team player ability, liaising directly with client and other project key functionsPrevious experience as manager/leader of C&Q teamStrong knowledge of ISPE and ASTM E2500Proven experience with international pharmaceutical projectsMentor for junior staff membersPackageCompetitive hourly rate of €65 - €75 per hourMinimum Contract of 12 months Hybrid Working


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