Automation Engineer - Dublin, Ireland - 6 Months Contract
How would you like the opportunity to work with in one of the largest bio-pharmaceutical projects in the country? If yes, then this is the assignment for you!
Our client is currently seeking the skills of an Automation Engineer to join their team. Our client develops and delivers life-changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!
Essential Duties and Responsibilities for this role include, but are not limited to, the following:
* URS’s GEP and GMP Automation part only
* System upgrade requirements – GEP and GMP Automation part only
* Agreed recipe handling functionality
* Voice Data and communications documentation IFD (process)
* Control System Architecture and User Requirements IFD
* System Architecture drawing
* Process Automation System Architecture IFD
* Setting and agreeing the Automation Design Philosophy, in alignment with the Automation and IT strategies, technical standards and guidelines and local realities and expectations.
* Setting and agreeing the automation parts of the project deliverable list, including the Automation and IT RACI.
* Providing technical guidance to C&Q, and CSV throughout the project.
* Lead the Automation User Requirements in alignment with relevant standards and guidelines.
* Champion the timely engagement, review and approval of URSs with Customer team.
* Supporting the Project Manager, Technical Project Manager, Work Package Owners, other SME’s with interpretation of the agreed Automation Design Philosophy and User Requirements.
* Supporting the Design Contractor(s) and Vendor(s) with translation of the agreed Automation Design Philosophy and User Requirements into Engineering deliverables.
* Establishing the resource estimates for the part of the automation delivery through all CPDP stages.
Desirable Experience:
* Pharma experience
* Writing URS’s
* Stakeholder management
* Reviewing and Approving SAT’s & FAT’s
* Process Automation
If this role is of interest to you, please apply now!
#LI-SC1 #J-18808-Ljbffr