CQV Engineer
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| Job Type | Contractor |
| Area | Limerick, Ireland |
| Sector | EngineeringQuality |
| Start Date | |
| Advertiser | David Connolly |
| Job Ref | 2813 |
| Job Views | 574 |
- Description
- CQV Engineer
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.
