Job Details: Commissioning Engineer


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.
Commissioning Engineer


Are you a C&Q Engineer (upstream) with experience in Pharma, Biotech or Medical device industries? Would you like to work for an International consultancy who provide an outstanding work environment and opportunities for career development? If you have what it takes, send your CV to  or call (01)7978720 for a confidential chat.



C&Q Engineer - Upstream Processing - Cork



Job Description



The C&Q Engineer shall be responsible for carrying out the following project related activities associated with Up-stream Process equipment: Bioreactors, Buffer vessels, mobile vessels. 

Preparation of documents associated with lifecycle of C&Q activities IV, FT, IQ, OQ. 

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 

Installation Qualification execution 

Operational Qualification execution 

Change Management activities during project lifecycle 

Summary Report writing 

Interfacing with representatives on project team, Construction, Engineering, Automation, Quality and End Users during the different project phases. 



Requirements:



Degree in Science or Engineering (or equivalent experience) 

5 years working in Biopharma engineering , operations, or manufacturing 

5 years in CQ experience 

Demonstrated team work abilities 

Knowledge of GMP’S, regulatory requirements, equipment commissioning and qualification 

Good written and verbal communication skills 

High attention to detail.



Package:

Contract rate of €35 - €45 per hour

Minimum Contract duration: 12 months



Contact:

Karen McHugh is the consultant managing this position. If you have any queries about this role, you can contact Karen by e-mail karen or phone +353-1-7978720

Click to connect with Karen on LinkedIn



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Jobs in Cork

Validation Jobs

Are you a C&Q Engineer (upstream) with experience in Pharma, Biotech or Medical device industries? Would you like to work for an International consultancy who provide an outstanding work environment and opportunities for career development? If you have what it takes, send your CV to  or call (01)7978720 for a confidential chat.



C&Q Engineer - Upstream Processing - Cork



Job Description



The C&Q Engineer shall be responsible for carrying out the following project related activities associated with Up-stream Process equipment: Bioreactors, Buffer vessels, mobile vessels. 

Preparation of documents associated with lifecycle of C&Q activities IV, FT, IQ, OQ. 

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 

Installation Qualification execution 

Operational Qualification execution 

Change Management activities during project lifecycle 

Summary Report writing 

Interfacing with representatives on project team, Construction, Engineering, Automation, Quality and End Users during the different project phases. 



Requirements:



Degree in Science or Engineering (or equivalent experience) 

5 years working in Biopharma engineering , operations, or manufacturing 

5 years in CQ experience 

Demonstrated team work abilities 

Knowledge of GMP’S, regulatory requirements, equipment commissioning and qualification 

Good written and verbal communication skills 

High attention to detail.



Package:

Contract rate of €35 - €45 per hour

Minimum Contract duration: 12 months



Contact:

Karen McHugh is the consultant managing this position. If you have any queries about this role, you can contact Karen by e-mail karen or phone +353-1-7978720

Click to connect with Karen on LinkedIn



Similar Jobs

Jobs in Cork

Validation Jobs

We need : English (Good)

Type: Permanent
Payment: package
Category: Pharmaceutical

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