Operations Engineer (Full Time)
Limerick, Ireland

The ultimate purpose of technology teams in GxP environments is to serve the evolving needs of the business. We are a specialist provider of consultancy and implementation services for IT infrastructure and data architectures within life science manufacturing. Our role is to be a companion on the road for technology teams to be able to use as a tool at times when decisions need to be made.

We now have an amazing opportunity for an Operations Engineer to join our growing team and work on site with our blue-chip multinational clients within the pharmaceutical industry. This role is based out of one of our client sites in Limerick.

The Position:
As an Operations Engineer, you will play a critical role working on manufacturing Vendor Package Equipment, Multiple SCADA Platforms and a variety of PLC’s and embedded controllers.
  • Contribute to the completion of projects, manage your own time to meet agreed targets and develop plans for short-term work activities on your own projects.
  • Developing automated system life cycle documents to meet cGMP requirements (i.e. SOPs, Configuration Specifications, Functional Design Specifications).
  • Supporting department audit\inspection readiness and participate in audits and regulatory inspections as required.
  • Ensure that work performed is compliant with GMP regulations, and Regulatory Agency requirements.
  • Implementing code/systems changes on the automation systems under change management/change control as part of sustaining and capital projects as required.
  • Work on production systems continuous improvement initiatives.
  • Maintain the validated state of the automation systems.
Previous Experience with :
  • A minimum of 3- 4 years’ experience in a similar role, coupled with a Electrical, Electronic, Systems Engineering, Computer Science or equivalent.
  • Extensive experience with Rockwell platform on PLC and HMI – Studio and FTView SE and ME.
  • Generation of Technical evaluations and test plans for change controls and comfortable checking code in and out of Assetcentre and operating ThinManger, PlantPAX experience is a big advantage.
  • Knowledge of GAMP software development lifecycle, ANSI/ISA-S88 and S95 industry standards and 21 CFR Part 11.
  • Previous experience in a regulated biopharmaceutical environment is a must.
  • Must hold a full valid Irish work permit as this role has an immediate start.
About us:

Oleson is a technology strategy & transformation practice. We are uniquely focused on IT/OT systems in manufacturing operations with a particular strength in regulated life sciences manufacturing. You already have trusted control system and applications vendors. Our strength is in taking a full system view and understanding the complex relationships between

– Manufacturing operations
– Business continuity
– IT infrastructure
– Compliance & change control
– System lifecycle planning

We have developed our own knowledge and process to ensure your IT/OT systems directly drive your business needs. We are ready to provide strategic advice or specific implementation services. To deliver successful projects you can use our capabilities selectively to augment the capabilities of your own project delivery team. We have a vast amount of experience in complex capital projects IT/OT projects in manufacturing operations.- 

To find out more about what we do visit our website here – https://oleson.io/



Don’t worry if there isn’t a current opportunity that suits your own expertise and interests. Positions arise with us for experienced
professionals on an ongoing basis. To register your interest for future roles that arise within our team, please email recruitment@oleson.io

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