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Senior CQV Engineer

  • Location: Dublin
  • Salary: €65.00 /hour
  • Job Type:Contract

Posted 24 days ago

  • Sector: Advanced Facilities
  • Contact: Duncan Lowe
  • Contact Email: dlowe@nrl.co.uk
  • Contact Phone: 01483 400 786
  • Start Date: ASAP
  • Expiry Date: 02 December 2021
  • Job Ref: 1038349
NRL are currently recruiting for a Senior CQV Engineer to work with a client of ours in Ireland. The role will be a contract position, based in Dublin with opportunities to work remotely.

 

Role Responsibilities:
  • 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
  • Organise 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.
 

Role Requirements:
  • A degree in science or engineering or equivalent.
  • A certificate/diploma in similar areas with appropriate industrial experience
  • Previous 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
 

What’s in it for you:
  • Stable contract duration
  • Competitive hourly rate