Project Engineer- Automation

12 month contract opportunity for Cork based Automation Engineer with a Pharmaceutical Manufacturer. Responsible for revalidating multiple fully automated production lines. This role requires a strong emphasis on documentation and compliance with industry standards.

Key Responsibilities

• Revalidate automated production lines for industry compliance.
• Develop and execute IQ/OQ/PQ validation protocols.
• Maintain accurate documentation of validation activities.
• Collaborate with teams to meet validation requirements and timelines.
• Troubleshoot and resolve validation and equipment issues.
• Oversee the introduction and validation of new equipment.
• Identify and implement equipment improvements (automation, robotics, etc.).
• Define equipment requirements with Product Development for new products.
• Review equipment proposals and vendor selections.

Skills & Experience

• Level 8 Bachelor's degree in Engineering, Science, or a related discipline.
• Demonstrated experience in validation within the medical device or pharmaceutical sectors.
• Knowledge of automated production equipment, such as Cognex and Keyence vision systems, and Epson and UR robots.
• Proficient in documentation and technical writing