Location: Ireland
Job Type: Contract
Industry: Biotech-Pharma-Medical-Device-Jobs
Job ID: JO-2211-31455
Consultant: Claire Doyle
Are you a CQV Engineer with a minimum of 5 years experience of C&Q activities in a large project environment within the pharmaceutical or biotech industries and have 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 ?
If you have the relevant experience, please forward your CV to karen@jobcontax.com for review or call 353 1 7978720 to discuss in confidence.
CQV Engineer - Pharma - Ireland
Job Description
Our client is an international engineering and PM consultancy with Life Science projects across Ireland.
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.
Requirements
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
Package
Competitive hourly rate of €45 - €55 per hour
Minimum Contract of 12 months
Contact
Karen McHugh is the consultant managing this position.
If you are CQV Engineer interested in roles based in Dublin and Ireland, you can contact Karen by e-mail at Karen@jobcontax.com Karen or phone 353 1 9696683 for a confidential chat.
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With over 50 years of technical recruitment experience, JobContax is the leading recruiter of CQV Engineers in Dublin and Ireland.
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