Project Engineer- Automation
12 month contract opportunity for Cork based Automation Engineer with a Medical Device 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
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
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