Senior Pharmaceutical Automation Specialist

4 days ago

Cork, Cork, Ireland beBeeAutomation Full time €80,000 - €120,000

The role of a Technical Coordinator is a critical position in ensuring the efficient and compliant automation of pharmaceutical API manufacturing processes. The Technical Coordinator will be responsible for managing and coordinating all technical activities related to the Emerson DeltaV Distributed Control System (DCS) Hardware and Software delivery.

Key responsibilities include:

  • Managing technical queries log and updates.
  • Coordinating software delivery to meet site DSAT dates.
  • Maintaining schedule adherence and mitigating any delays.
  • Supporting validation, regulatory compliance, and continuous improvement initiatives critical to Good Manufacturing Practices (GMP).

The ideal candidate will have extensive experience with Emerson DeltaV DCS in a pharmaceutical or highly regulated manufacturing environment. Strong knowledge of pharmaceutical manufacturing processes and regulatory requirements is essential. Experience with system validation lifecycle (IQ/OQ/PQ) and documentation practices is also required.

Responsibilities
  • Serve 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.
Requirements
  • 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).
Location

Tipperary, Ireland

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