Project C & Q Engineer


Apply for this job

Location: Dublin

Type: Permanent

Salary: Negotiable


Reference: CQV BIO

Updated: 11/09/2018 15:50:13

Primary Purposes of Position

The purpose of the role is to generate/review & execute C&Q documents for a new automated process on our Clients site.

Long term Contract: 2yrs
Hourly Rate: Negotiable depending on experience
Start Date: September/October 2018

Main Duties to be Performed:

•Write & Execute Commissioning Dossiers.

•Assist with the Generation MSCR's (Maintenance System Change Request) at project handover.

•Project Planning - Manage the planning of the C&Q phase of the project to meet key milestones.

•Co-ordinate cross functional meetings to meet the objectives including Site Change Control Process.

•Report project C&Q performance on a regular basis to Project Manager using our Clients project reporting systems.


Ideal: 15yrs
Minimum: 10yrs

(5+ years Pharma experience as a Commissioning and Qualification Engineer
5+ years experience in generating and executing SATs, IQs, OQs for process equipment and process pipework in API plants)

Extensive experience in reviewing Construction Handover Documentation for Mechanical Pipework Systems and Equipment handover documentation
Experience with DCS or PLC/SCADA automation systems


Degree qualified in Mechanical / Process Engineer

Apply for this job

« Return to previous page