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Deltav project engineer 1629

Dublin
Simotechnology
Project engineer
Posted: 27 November
Offer description

What is it like to work at SimoTech?
With astrong collaborative teamwork culture based on respect, trust and excellence,we play a critical partnering role to our clients' life-changing supply ofproducts to patients.
In return, there is excellent salary, benefits, careerprogression, educational support and much more.
SimoTech have an opportunity for a DeltaVProject Engineer to join our team, supporting our client on theirstate-of-the-art biotechnology manufacturing site in Dublin.
The role sits onthe NPI (New Product Introduction) team and reports to the Automation Lead.
Thesuccessful candidate will work as part of the core engineering team, supportingmultiple key projects.
The ideal candidate will have 5+ years'experience as an Automation Engineer in the life sciences industry, workingwith Emerson DeltaV and/or PLC/SCADA systems.
KeyResponsibilities
Be a keymember of the NPI site project team, contributing to multiple projects.
Coordinatewith Process SMEs, CQV Leads, and Automation Engineers to understand processrequirements.
Liaisewith all relevant stakeholders to gather all key technical inputs forFunctional Design Specifications (FDS).
Provideinput, review and sign off on functional design aspects, as and when required.
ImplementACPs (Automation Change Pack) to enable the required code changes.
Participatein internal project reviews with key stakeholders within automation and with customers.
Requirements
Bachelor'sDegree in Engineering, Sciences or equivalent.
5+years of working experience as an Automation Engineer in a highly regulatedbiotechnology environment.
5years' experience with DeltaV batch automation and/or PLC/SCADA systems, withknowledge of the integration between DeltaV and PLC/SCADA systems desirable.
Abilityto interact and communicate with other engineering and business disciplines,including Process Engineers, to define project scopes and deliver on project specifications.
Knowledgeof automation compliance lifecycle and change management.
Priorprocess plant commissioning experience.
Goodunderstanding of life sciences regulations and compliance requirements includingGAMP, 21 CFR Part 11 and the S-88 Batch Standard is a must.
Stronginterpersonal and communication skills are required, with a proven ability tocommunicate and build relationships cross-functionally.
Role provides a high degree of autonomy to allow the successfulcandidate to reach their full potential.
Develop new skills and enhance technical ability by working withinnovative technologies in a multi-disciplined environment.
Opportunity to work with large corporate clients on exciting capitalprojects.
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