CQV Engineer (Upstream/Downstream)


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https://www.teamhorizon.ie/job-search/385-cqv-engineer-upstream/downstream/engineering/dublin/job2022-01-06 17:49:131970-01-01Team Horizon
Job TypeContractor
AreaDublin, IrelandDublinIreland
SectorEngineering
Start Date
AdvertiserAshling Guthrie
Job Ref#2309
Job Views154
Description
Team Horizon currently has an exciting opening for a CQV Engineer to work on Upstream, Downstream and Process Utilities. This role allows an opportunity to join a team for the execution phase on dynamic project for blue chip bio pharma client.

 

What you will be doing:



  • 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 protocols


  • Preparation and execution of Qualification protocols (IQ and OQ)


  • Design Review (DR) and Design Qualification (DQ) protocol preparation, execution and follow-up


  • Field Walkdowns of systems as part of transfer of ownership of the system from Construction


  • Ensuring safe operation of the system prior to and during start-up functional testing and Qualification phases


  • Installation Verification execution


  • System Startup activities


  • Functional Testing of systems


  • Change Management activities during project lifecycle


  • Summary Report writing


  • Organize and review daily tasks/verifications and track the progress of the activities assigned


  • Contractors and/or Vendors coordination


  • Interfacing with representatives on project team, Construction, Engineering, Automation, Quality and End Users during the different project phases.


 

What you need to apply:



  • Minimum 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: Black & Clean Utilities, Purification Equipment, Reactors, Filtration equipment, CIP, Upstream process, Downstream process etc.


  • Experience with Regulatory and industry standards for GMP and GEP


  • Self-starter & good team player


  • Good oral & written communication skills


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