Automation Engineer

If you are a current Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.

The Automation Engineer is part of the global automation engineering Function. He/She is responsible for carry out improvement activities, provide maintenance support for existing Manufacturing Process Control Systems and to develop ,sup port new Process Control , Safety Systems deployments across Jazz internal Manufacturing sites. This role ensures the activities carried is aligned with global automation and site specific standards in the design, delivery and deployment. He/she will also be responsible as part of the global automation team to support project and maintenance support of other internal manufacturing sites. Essential Functions/Responsibilities Ensure that deployed systems are available for Manufacturing, maintained, and their qualified status is not compromised. Assist in Design and implementation of Hardware and Software solutions in accordance with Standard Operating Procedures and the Automation standards. Cooperate with the Site Engineering, QA and IS Compliance departments to ensure production continuity and fast problem resolutions. Tasks such as audits, CAPAs and validation testing are completed on time successfully and as priority, in particular: Cooperate with the Manufacturing team, ensuring all system changes are communicated ahead of time and that production schedule is accounted for. React quickly to reports of Manufacturing system faults, troubleshoot in collaboration with Manufacturing and the other Engineering disciplines. Assist in the development software and hardware configuration to remediate system faults or errors, improve efficiency and safety, as requested and in response to CAPA or Error report actions. Carry out preventative and planned maintenance activities on time and suggests/identifies maintenance requirements where needed. Carry out system modifications in accordance with the appropriate Change Control procedure. Actively identify & pursue process quality, efficiency, and safety improvements. Seeking out opportunity to improve understanding and to raise the profile of the Automation team. Ensure all Quality & Compliance tasks are completed on time and as priority. Carryout all responsibilities as detailed within applicable Global/Site SOPS available on Jazz EQMS relevant to the task. The job holder is responsible for maintaining cGxP and H&S knowledge applicable to the job. Manage third party vendors to the interest of Jazz Pharmaceuticals For his/her Area of competence, he/she carries out the operating procedures for the management of his/her activity in compliance with the Principles of the Environmental Policy and the Quality System, applies the relevant guidelines and indications contained in the procedures of the Environmental Management System of his/her competence. Participates in the training and education courses in the field of the Automation, Environmental, Safety and Quality Management System and in the training courses on Procedures, Instructions, Manuals and Operating Protocols. He/She is responsible for carrying out