descrizione del lavoro

pbIf you are a current Jazz employee please apply via the Internal Career site. /b /p pJazz 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 for more information. /p ppThe Manager of Automation Engineering is responsible for leading and overseeing the implementation of automation technologies and strategies in the Villa Guardia manufacturing site within a GxP environment, to improve efficiency and to keep the manufacturing at the best industry standards in cooperation with the Global Engineering and with the Automation Engineering of the Internal Manufacturing sites. He/She is responsible for the Building Process Automation improvement activities, to drive the new Process Control and Safety Systems deployments across Villa Guardia Site and to provide maintenance support for the existing Manufacturing Process Control Systems. /ppbEssential Functions/Responsibilities /b /pullipDesign and implement Hardware and Software solutions in accordance with Standard Operating Procedures and the Global Automation Policy. /p /lilipCooperate with the Global Engineering, Internal Manufacturing sites Automation Engineers and IS for the TechOps Automation Roadmap implementation, including the definition of the automation systems interfaces with the IT infrastructure. /p /lilipSupport the Site Engineering in the activities of specification and follow up of pharmaceutical plants and equipment using established procedures. These include equipment selection, schematic design, system layout, cost estimation and system documentation. /p /lilipDevelop and implement control and automation design based upon cause-and-effect documentation, PIDs, control narrative and an understanding of the environment. /p /lilipEnsure accuracy and reliability of instrumentation, control and safety systems. /p /lilipActively identify pursue process quality, efficiency, and safety improvements, by maintaining cGxP and HS knowledge applicable to the job and by assessing them against of the “State of the Art” technology. /p /lilipWrite and update SOPs and other Process Control System associated documentation as part of the operational lifecycle. /p /lilipCooperate with the Site Engineering, QA and IS Compliance departments to ensure production continuity and fast problem resolutions and tasks such as audits, CAPAs and validation testing are completed on time successfully and as priority. In particular: /pullipEnsure that deployed systems are available for Manufacturing, maintained, and their qualified status is not compromised. /p /lilipCooperate with the Manufacturing team, ensuring all system changes are communicated ahead of time and that production schedule is accounted for. /p /lilipReact quickly to reports of Manufacturing system faults, troubleshoot in collaboration with Manufacturing and the other Engineering disciplines. /p /lilipAssist 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. /p /lilipCarry out preventative and planned maintenance activities on time and suggests/identifies maintenance requirements where needed. /p /lilipCarry out system modifications in accordance with the appropriate Change Control procedure. /p /li /ul /li /ulpFor 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. /ppParticipates in the training and education courses in the field of the Environmental, Safety and Quality Management System and in the training courses on Procedures, Instructions, Manuals and Operating Protocols. /ppHe/She is responsible for carrying out his/her activities so that the management of environmental and safety aspects is conducted correctly. Carries out the work activities, in compliance with the directives received, as required by Legislative Decree 81/08 Guarantees compliance with all applicable Laws, Codes, company standards and Procedures relating to his/her area of competence, particularly the requirements of the Jazz Pharmaceuticals Code of Conduct. /ppbRequired Knowledge, Skills, and Abilities /b /pullipAdvanced knowledge of Distributed Control and Safety Systems and/or PLC applications. /p /lilipAwareness of integrated process control SIMATIC Batch (batch processing). /p /lilipGood demonstratable knowledge of Batch process. /p /lilipWorking knowledge of GAMP and GEP. /p /lilipDatabase administration experience (SQL). /p /lilipAdvanced PLC programming skills (eg STL, SCL). /p /lilipHigh level programming eg: C, C++, VB etc. /p /lilipCompleted structured system testing and documentation such as FAT/SAT/OQ protocols. /p /lilipFollowed system maintenance programmes. /p /lilipCompleted system version upgrades. /p /lilipCapability to install, configure and update Process Control System software (Siemens brand is preferred). Experience of Siemens products (e.g. PCS7). /p /lilipExperience in maintaining and upgrading PLC or DCS control systems. /p /lilipExperience in designing, maintaining and upgrading network infrastructures /p /lilipSoft skills: /pullipAble to form long term relationships with key support groups, QA, engineering, CSV group and senior managers across the site. /p /lilipShares ideas and information and acts in a transparent manner /p /lilipDemonstrates a ‘can do’ approach. /p /lilipWilling to learn new technologies and their application relevant to the job /p /lilipFluent English /p /lilipGood oral, written and presentation skills essential /p /li /ul /lilipFollowing capabilities will be considered a valuable plus: /pullipExperience on the installation, configuration and updating of Process Control System software from major vendors other than Siemens (ABB, Emerson, Rockwell etc.) /p /lilipExperience in the Pharmaceutical Industry /p /lilipExperience of Safety Instrumented Systems /p /lilipExperience of commissioning activities /p /lilipOperational Excellence / Lean manufacturing skills and/or certifications (i.e: Green or Black Belt) /p /li /ul /li /ulpbRequired/Preferred Education and Licenses /b /pullipMaster’s degree in engineering, Electrical, Automation or any relevant technical education /p /lilip7 ÷ 10 years’ experience of PLC based unit operation including graphical interface and data collection /p /li /ul /p pemJazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. /em /p The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .