Website Asset Recruitment

Asset Recruitment

Job ref: 339586

Greenfield Veterinary Biologics Manufacturing Facility based in Tullamore.

Offers hybrid working

Contract runs until November 2023

Responsibilities: 

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.

Key Competencies: (Education, Training, Skills, Experience)

  • A degree in science or engineering or equivalent OR certificate/diploma in similar areas with appropriate industrial experience
  • 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
  • Experience with Regulatory and industry standards for GMP and GEP
  • Self starter & good team player
  • Good oral & written communication skills
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