Job Description:
A Project Engineer is required to implement an effective manufacturing process. This involves providing technical and engineering maintenance and calibration support for equipment and fixture solutions that optimize manufacturing practices.
Key Responsibilities:
* Introduce and validate new equipment.
* Collaborate with Value Streams to improve equipment, including automation, vision systems, and robotics.
* Work with Product Development to establish equipment requirements for new products.
* Engage with external vendors to review equipment proposals and select vendors.
* Identify and resolve production/engineering issues with cross-functional teams.
* Validate new equipment, ensuring Maintenance and Calibration requirements are incorporated into specifications.
* Transfer and validate equipment from other sites.
* Debug production issues with automated equipment.
* Maintain relevant documentation in accordance with Quality and Regulatory guidelines, ensuring compliance with GMP and E&AS requirements.
Requirements:
* Bachelor's or Master's degree in Engineering, Science, or a related discipline.
* 3-4 years of experience in a similar role within a GMP regulated environment.
* Prior experience in Medical Devices is advantageous.
* Excellent communication and analytical skills with the ability to work collaboratively.
* Proven ability to multitask and handle competing priorities effectively.
* Strong technical aptitude and problem-solving abilities.
* Cork-based role with 5 days a week on-site requirements.