12 month contract opportunity for Cork based Automation Engineer with a Pharmaceutical Manufacturer.
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.
Requirements
* 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.