Automation Engineer – Athlone
About the Job
Oleson specialises in delivering high-quality talent and solutions that enhance the capabilities and operational excellence of our global customers.
We are focused on matching the dynamic needs of Data Centre and Life Science clients with skilled professionals, thereby driving innovations and in growth in these critical sectors.
Role Description:
The Automation Engineer is responsible for configuration, operation, maintenance, and administration of the process and facility control and data historian systems to cover all manufacturing systems at our clients site including supporting Utility (GMP and GEP) from a sustaining perspective.
What you’ll do:
Work independently, or with third party system integrators, to configure and implement all automation systems onsite.
Manage third party vendors/system integrators either for project or sustaining activities.
Give guidance to our in-house Automation team on all automation systems in the Manufacturing Facility
Develop, review and approve design documentation
Develop, review and approve all project standards
Provide automation expertise to the engineering and operations department on design and sustaining decisions
Develop and implement standard operating procedures to ensure the future compliance and management of all automation systems
Ensure all automation systems are delivered and maintained in a compliant and qualified state
Provide support for all validation activities
Participate in cross-functional teams to ensure a high level of optimization for all equipment.
Assist in training personnel on specific automation aspects of equipment
Design and implement solutions across various automation platforms in line with the automation/site change control procedures
Where required, lead an Automation project team to deliver inhouse projects.
Lease with project leads to deliver to work on project priorities and timelines.
On occasion, where required take on delegate responsibilities from Senior Manager, Manufacturing Systems.
The Requirements:
Degree in Engineering/Computer Science or equivalent
8 years + within the automation industry supporting GMP environments and applications
Experience supporting a Fill Finish facility
Direct experience and in-depth knowledge of Siemens TIA (and non-TIA), WinCC, Desigo, AVEVA (formally Wonderware) Intouch & Historians.
Experience in managing and working alongside system integrators
Direct experience in supporting a manufacturing facility
Develop scope and estimations to support NPI projects
Experience maintaining controls networks and communications by Profibus and Ethernet.
Experience with OSI PI data historian, SQL Server and virtualization platforms is a plus, as is IT experience.
Experience of implementing change controls and investigating deviations/events.
Comprehensive understanding of cGMP requirements for clinical and commercial biopharmaceutical manufacturing and the ability to implement best practices (GAMP) to ensure site automation systems are cGMP compliant.
