We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. 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.

Our client is seeking a System Owner Engineer to support the installation, validation, and lifecycle management of automated syringe inspection systems within a GMP fill-finish facility expansion.

This role will focus on vision systems, reject mechanisms, and inspection performance optimisation.

Key Responsibilities:

• Act as System Owner (SO) for automated syringe inspection systems.
• SO during the FAT/SAT, commissioning, qualification, and validation activities.
• Ensure compliance with GMP, Annex 1, and data integrity requirements.
• Own system performance metrics including: False reject rates, Detection capability, OEE performance
• Support inspection recipe development and optimisation.
• Develop maintenance and lifecycle strategies for inspection equipment.
• Lead troubleshooting and root cause investigations for inspection failures.
• Support audit readiness and regulatory inspections.

• Bachelor’s Degree in Engineering (Mechanical, Electrical, Automation, or related discipline).
• 5+ years’ experience in biopharmaceutical manufacturing.
• Experience with: Automated visual inspection systems (AVI), Vision systems, High-speed packaging or inspection lines
• Understanding of particulate detection, cosmetic defect inspection, and container closure integrity.
• Experience supporting equipment validation and data integrity compliance.
• Strong analytical and problem-solving skills.