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CQV Engineer
Team Horizon is seeking a CQV Engineer for a role based in Limerick with a leading engineering company.
Why you should apply:
What you will be doing:
What you need to apply:
Team Horizon is seeking a CQV Engineer for a role based in Limerick with a leading engineering company.
Why you should apply:
- Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
- You enjoy working on exciting projects and want to work with a global manufacturing site in Cork
- Excellent contracting rates
What you will be doing:
- 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:
- A degree in science or engineering or equivalent. Or A 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, 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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