CQV Engineer (Upstream/Downstream)
This job does not exist anymore.
Try running a new searchor browse our vacancies.
Or fill in the form below to receive job alerts.
Job Type | Contractor |
Area | Dublin, Ireland |
Sector | Engineering |
Start Date | |
Advertiser | Ashling Guthrie |
Job Ref | #2309 |
Job Views | 154 |
- Description
- Team Horizon currently has an exciting opening for a CQV Engineer to work on Upstream, Downstream and Process Utilities. This role allows an opportunity to join a team for the execution phase on dynamic project for blue chip bio pharma client.
What you will be doing:
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.
What you need to apply:
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