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Rachel Kent
Life Science

+353 87 427 8808
[email protected]
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Details

DeltaV Technical Coordinator - Hybrid


Reference:RK23749 Location: Tipperary
Qualification:DegreeExperience:4-5 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Technical Specialist

DeltaV Technical Coordinator - Hybrid
RK23749
Contract – 11 months
Tipperary



We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Tipperary. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.


The Delta V Technical Coordinator is responsible for managing and coordinating all technical activities related to the Emerson DeltaV Distributed Control System (DCS) Hardware and Software delivery to ensure compliant, reliable, and efficient automation of pharmaceutical API manufacturing processes



Duties:

  • Liaising with multiple cross functional Agile teams of System Integrators, Site Process and Operation Teams, Automation Engineers on a day-to-day basis to manage the progress of the sprint and to remove any roadblocks or impediments that the team is facing.
  • Coordinate with the Scrum Master, Product Owner and System Integrator on a day-today basis to plan every sprint.
  • Manage Technical Queries Log and updates
  • Manage escalations to DeltaV Workstream Lead and PM as requiredServe as the primary technical point of contact for all DeltaV DCS-related projects and operations within pharmaceutical manufacturing facilities.
  • Lead the implementation, configuration, and validation of DeltaV systems in accordance with FDA regulations, 21 CFR Part 11, and GMP guidelines.
  • Develop, configure, and test DeltaV control strategies, logic, and operator interfaces to meet pharmaceutical process requirements.
  • Provide expert troubleshooting and root cause analysis for DeltaV system issues, ensuring minimal downtime and compliance with quality standards.
  • Maintain detailed documentation including system design specifications, validation protocols (IQ/OQ/PQ), change control records, and SOPs to support audits and regulatory inspections.
  • Train operators, engineers, and maintenance personnel on DeltaV system operation, change management, and compliance requirements.
  • Collaborate with Emerson, system integrators, and quality assurance teams during audits, inspections, and vendor assessments.
  • Identify and implement system enhancements to improve process control, data integrity, and operational efficiency while maintaining compliance.
  • Participate in risk assessments and mitigation planning related to control system changes and upgrades.
  • Ensure Automation compliance with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.


Educational and Experience
  • Bachelor’s degree in Electrical Engineering, Instrumentation, Automation, or related technical field.
  • Extensive experience with Emerson DeltaV DCS in a pharmaceutical or highly regulated manufacturing environment.
  • Strong knowledge of pharmaceutical manufacturing processes and regulatory requirements (FDA, EMA, 21 CFR Part 11, GAMP 5).
  • Experience with system validation lifecycle (IQ/OQ/PQ) and documentation practices.
  • Proficiency with DeltaV software tools (Control Studio, AMS Suite, DeltaV Operate).

If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.