Automation Engineer
- Ireland, Dublin
- Contract
- CAPEX Projects
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 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.
- Pharma experience
- Writing URS’s
- Stakeholder management
- Reviewing and Approving SAT’s & FAT’s
- Process Automation
#LI-SC1
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
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