Job Details: Senior CQV Engineer - Biotech - Cork


jobContax

104 Upper Drumcondra Road,
Dublin 9
http://www.jobcontax.com
Please contact: Karen
JobContax was founded in 2001 by Karen McHugh, an engineer passionate about offering quality opportunities to the jobseeker and an intelligent service to the client. Jobcontax has successfully operated as a global market leader and technical specialist within the following sectors:

Construction and Infrastructure

Engineering and Design

Mining - Oil and Gas

Biotechnology and Pharmaceutical

During the past 10 years Jobcontax have expanded our international network across 5 continents. In 2005 we began recruiting for the Australian market and in 2011 we set up our first strategic partnership in WA. In March 2010, we opened our Shanghai office to strengthen our presence in the rapidly expanding Chinese market for highly skilled professionals. JobContax has a strong presence in Canada, Europe and the Middle East.

Jobcontax has built its reputation on its consultative approach. Our understanding of the industries and the businesses and individuals within these industries enables us to facilitate the perfect match between client and jobseeker. From global multinationals to SME?, Jobcontax has become the trusted recruitment partner.
Senior CQV Engineer - Biotech - Cork
Are you a Senior CQV Engineer with API experience of full life cycle
activities incl. doc prep, change control and protocol execution on
grey utilities and HVAC?

If interested in this role, call Claire on + *
* to discuss or forward your CV to **Apply on
the website** for review

SENIOR CQV ENGINEER - BIOTECH - CORK

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. 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: API
Facilities, Grey Utilities, HVAC

Experience with Regulatory and industry standards for GMP and GEP

Self starter & good team player

Good oral & written communication skills

PACKAGE

Hourly rate of € * - €**Apply on the
website** per hour



We need : English (Good)

Type: Permanent
Payment: EUR 65 - 75 Per Hour
Category: Construction

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Please Provide a Cover in the English Language.
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