CQV Engineer
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Job Type | Contractor |
Area | Cork, Ireland |
Sector | EngineeringQuality |
Start Date | |
Advertiser | David Connolly |
Job Ref | 1002813 |
Job Views | 555 |
- Description
- CQV Engineer
Team Horizon is seeking a CQV Engineer for a role based in Cork with a leading engineering company. The CQV Engineer is required to work on site in a small team as part of a small projects group resident on site.
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.
And any other duties as assigned.
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.