Senior CQV Engineer
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 | Tipperary, IrelandWaterford, Ireland |
| Sector | EngineeringIT/Software |
| Start Date | |
| Advertiser | David Connolly |
| Job Ref | 1002875 |
| Job Views | 646 |
- Description
- Senior CQV Engineer
Team Horizon is seeking a Senior CQV Engineer for a leading engineering company in Tipperary.
Senior CQV Engineer must have Isolator experience. This role is full time on-site.
Why you should apply:
You enjoy working on exciting projects and want to work with a global manufacturing site in Tipperary.
Excellent contracting rates on offer
You enjoy working in a culture of learning and collaboration and making a positive impact.
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.
And any other duties as assigned.
What you need to apply:
A degree in science or engineering or equivalent.
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.
