CQV Engineer Pharmaceutical Industry

Contact Aimee Burke
  • Salary: Negotiable
  • Location: MunsterCork
  • Sector: Pharma & Life Sciences
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CQV Engineer

Sonas Technical is currently partnered with a multi billion global-leading pharmaceutical client in search of an experienced CQV Engineer.  The successful candidate will will work on major €100+ million pharma project in Cork.

Why apply with Sonas ?

  • We can provide insights to the best salaries, rates and benefits on offer
  • One point of contact – We can manage all your applications, interviews and negotiations
  • We will get your CV seen by the right hiring managers

Key Responsibilities:

  • Creation of documents associated with lifecycle of C&Q activities for a IV, FT, IQ, OQ
  • Development 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 phase
  • Installation Verification execution
  • System Start-up 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 phase

Key Requirements:

  • Relevant 3rd level degree
  • 5 year’s experience of C&Q activities in a large project environment within the pharmaceutical or biopharma industries.
  • Delta V experience is advantageous.
  • Hands on expertise required in one or more of the following areas: Upstream/Downstream Process Manufacturing Equipment, Grey/Black Utilities or HAVC.
  • Experience with Regulatory and industry standards for GMP and GEP

A market leading remuneration package is available for the successful candidate.

To apply please email your CV to aimee.burke@sonastechnical.com or apply directly through Indeed

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