Infrastructure Engineer to join our client&#**Apply on the website**;s
large scale biologics manufacturing facility in Dublin.
The Automation Infrastructure Engineer shall be responsible, as part
of the client team, for the development and delivery of the IT
Infrastructure to support the Manufacturing (OEM, MCS, MES etc.)
Systems to enable the start-up, commissioning and qualification of our
client&#**Apply on the website**;s Bulk Drug Substance manufacturing
facility.
(file://humanresources/DavWWWRoot/glblvl/Global%**Apply
on the website**Leveling%**Apply on the
website**Criteria/Position%**Apply on the website**Description%**Apply
on the website**Guide%**Apply on the website**-%**Apply on the
website**ALXN%**Apply on the website**(2.2).docx#Qualifications)
* Degree level qualification in computer science, business information
systems, automation engineering or equivalent.
Technical skills
* Experience Administration of Microsoft Windows Sever **Apply on the
website** R2 and **Apply on the website**
* Good understanding of networking (VLAN, Switches, Routing)
* Experience with Active Directory infrastructure and administration.
* Experience with Windows Remote Desktop Services
* Experience administration of MES systems (Syncade)
* Experience with SQL Server **Apply on the website**
* Experience with VMWare 5.x/6.x
* Experience with Thin Client Software solutions
* 5 years&#**Apply on the website**; experience Administration of
DeltaV Batch Executive, Continuous Historian, Batch Historian, Asset
Management
* Experience in Cyber Security , Digital Immunity
* Experience in Acronis software (Backup and Disaster Recovery)
* 5 years&#**Apply on the website**; experience Administration of
DeltaV
Emerson training courses**Apply on the website** - DeltaV
Administration
* 5 years&#**Apply on the website**; experience Administration of
HyperV Clusters and DeltaV Virtual Studio
Emerson training courses **Apply on the website** - Virtual Studio
Administration
General Skills
* Thorough knowledge of Pharmaceutical Industry Regulations
(cGMP/cGLP, OSHA, EPA/EQB) is required
* Experience in the preparation of method statements, safe plans of
action and work permits
* Understanding of documentation, such as Hardware Design, Network
Design, FAT and SAT documentation
* Knowledge of cGMP particularly as it applies to biologics
manufacturing and automated systems
* Ability to keep work pace and meet deadlines. Good organizing and
planning skills
* Strong communication skills
* Problem solver with a focus on achievement of overall project goals
* Proven success working well in a team environment with flexibility
to react to changing business needs
* Ability to anticipate, evaluate and resolve multiple, simultaneous
project issues, delays and problems by utilising technical, project
management, and business expertise
* Ability to work independently and remotely with minimum direct
supervision
* Strong Critical thinking skills
* Ensuring compliance with practices, policies, procedures, legal
requirements and goals of project sponsors and approved methodologies,
develop supporting documentation and monitor budget tracking/
timeliness/ scheduled resources
We need : English (Good)
Type: Permanent
Payment:
Category: Others
