Responsibilities

• Reporting to the DeltaV Lead, supporting delivery of DeltaV scope on the project.
• Develop and/or review System Development Life Cycle (SDLC) deliverables, compliant with site standards.
• Work with DeltaV vendor in development of systems architecture, specifications, controls strategies, sequence of operations through all design stages.
• Work closely with the Quality function to ensure compliance with site Quality standards.
• Participate in Hardware and Software FATs and SATs, as required
• Provide input to the development of project schedules and document trackers.
• Participate in, and support, relevant project meetings.
• Liaise with stakeholders on the overall project to ensure clear communication between all parties.
• Experience in the Design of DeltaV for both Upstream and Downstream processes.
• Experience in the Design, Testing and commissioning of DeltaV site at a GMP manufacturing site.
• Technical proficiency on controls systems including familiarity with control panels, networking, panel/field wiring and PLC control systems.

Education

• Bachelor’s Degree in Engineering, Information Systems, Computer Science or the Life Sciences.
• Experience in a similar role, ideally in the Pharmaceutical industry.

To apply contact Martin Lynch on 087-344 3581.

Email CVs to mlynch@mile.ie