Your New Job Our client is a specialist Pharmaceutical Manufacturing firm that have a requirement for Automation Technician to be based in Waterford. They are seeking a candidate to join their growing team on a full-time, permanent basis. Must be available to work shift: rotating shift, 2 Days 2 Nights with 4 days off Key Duties & Responsibilities: Maintain and support the performance of automation equipment in accordance with health & safety, quality, and operational standards. Carry out systematic root cause analysis and troubleshooting to resolve equipment and process issues efficiently. Perform preventive and corrective maintenance activities, ensuring all maintenance records and documentation are completed accurately. Lead and support continuous improvement projects aimed at increasing equipment efficiency, yield, and reliability, while ensuring compliance with cGMP and change control processes. Assist in the commissioning and validation of new equipment and projects, including support for FAT, SAT, and IOPQ activities. Manage inventory of spare parts and ensure critical components are always available. Provide cross-training and technical support to technicians across the team as required. Participate in equipment buy-offs and training sessions, including occasional travel to vendor sites if needed. Ensure full compliance with all safety, quality, and regulatory programs and initiatives across daily operations. Maintain accurate records of all maintenance activities, adhering strictly to GMP standards and training requirements. Perform additional tasks as required in response to the evolving needs of the business and the automation department. What Are We Looking For? Minimum Level 6 qualification (or higher) in Manufacturing Technology, Mechanical/Automation Engineering, Electrical, Electronics, Mechatronics, or a related discipline. Qualified trades personnel with relevant industrial automation experience will also be considered. Proven experience working with high-volume automation and robotic systems is essential. Previous experience in a medical device or regulated manufacturing environment is highly desirable. Technical knowledge across areas such as Pneumatics, Hydraulics, Electronics, PLCs, Servo Motor Drives, Vision Systems, and Ultrasonic Welding is advantageous. Solid understanding of Process Capability, MSA, and GR&R principles. Experience in leading or supporting process improvement initiatives within a regulated manufacturing environment. Strong problem-solving skills, with a structured and methodical approach to fault finding and root cause analysis. Proficient in Microsoft Office and capable of using maintenance management and technical documentation systems. Excellent communication and interpersonal skills, with the ability to work effectively in cross-functional teams. Committed to working safely, accurately, and in full compliance with GMP and change management procedures. Apply for this job now by emailing your WORD formatted CV By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are kept confidential and will not be submitted to any clients without your knowledge and permission. Please note that due to the expected high volume of applications we can only reply to applicants suitable for the position. We Value Your Trust.