System Automation Specialist

3 days ago

Cork, Cork, Ireland beBeeAutomation Full time €90,000 - €110,000
System Automation Specialist

Job Summary:

We are seeking a skilled System Automation Specialist to join our team. This is an exciting opportunity for someone who wants to work with advanced automation systems.

The ideal candidate will have extensive experience with Emerson DeltaV DCS and a strong understanding of pharmaceutical manufacturing processes.

  • Responsibilities:
  • Manage and coordinate 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.
  • Coordinate with cross-functional Agile teams on a day-to-day basis to manage the progress of the sprint and remove roadblocks or impediments that the team is facing.
  • 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.
Requirements:

To be successful in this role, you will need:

  • Bachelor's degree in Electrical Engineering, Instrumentation, Automation, or a 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.
  • Experience with system validation lifecycle (IQ/OQ/PQ) and documentation practices.
  • Proficiency with DeltaV software tools (Control Studio, AMS Suite, DeltaV Operate).
About Us:

We are a leading multinational organization committed to excellence in pharmaceutical manufacturing. We offer a dynamic and challenging work environment with opportunities for growth and professional development.

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