Migration Expert

2 weeks ago


Mullingar, Ireland beBeeAutomation Full time €100,000 - €150,000
Senior Automation Migration Expert

Job Overview:

We are seeking a highly skilled Senior Automation Migration Expert to lead automation migration projects in a regulated pharmaceutical manufacturing environment.

  • Lead and manage multiple automation migration projects (PLC, SCADA, DCS, BMS, EMS, MES).
  • Define and execute migration strategies, timelines, and risk assessments.
  • Oversee technical delivery of systems including Autoclaves, Parts Washers and WIP/CIP Skids (Rockwell & Siemens).
  • Collaborate with operations, QA, validation, IT, and external vendors to ensure minimal production impact.
  • Ensure all systems are validated in line with GMP/21 CFR Part 11/Annex 11 and aligned with IQ, OQ, PQ documentation.
  • Mentor junior engineers and provide technical leadership to the automation team.
Key Responsibilities:

The Senior Automation Migration Expert will be responsible for:

  • Managing multiple automation migration projects simultaneously.
  • Defining and executing migration strategies, timelines, and risk assessments.
  • Ensuring all systems are validated and aligned with regulatory requirements.
  • Providing technical leadership to the automation team.
Requirements:

To be successful as a Senior Automation Migration Expert, you will need:

  • Bachelor's or Master's degree in Automation, Electrical, Mechatronics, Computer Science, or related field.
  • 7+ years' automation engineering experience, including 3+ years in a senior/lead role in pharma or biotech.
  • Proven expertise in system migrations from Siemens S7/PCS 7 and Rockwell Automation/Allen-Bradley.
  • Strong knowledge of GAMP 5, CSV, data integrity, and GMP standards.
  • Skill in industrial communication protocols (Profibus, Modbus, OPC UA, Ethernet/IP).
  • Excellent project management, stakeholder engagement, and documentation skills.
Why This Role?

This is an excellent opportunity to work as a Senior Automation Migration Expert and take on a challenging role in a regulated pharmaceutical manufacturing environment.



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