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I further attest that all information I submit in my employment application is true to the best of my knowledge. **Job Description** **_JOB PURPOSE:_** + SME in Manufacturing Control Systems, Operational Technology, Machine Automation and Digitalization + Act as system administrator for automation systems. + Monitor computerized systems performance to ensure maximum system uptime. + Manage system user access, backup and restore. + Troubleshooting and implementation of any corrective actions, including working with vendor technical support resources. + Support routine system patching programs. + Identify, plan and implement small projects to optimize system performance. + Participate/lead investigations related to control system deviations. + Support Site Automation & Digitalization projects – perform project-based tasks, such as: + Participate and make suggestions for capital planning, spending and tracking. + Participate in project teams representing your responsibilities. + Execute/document assigned project tasks within planned schedule and budget, this may include the installation/configuration of systems hardware/software, authoring/updating system documentation. + Carry out all assigned responsibilities in compliance with site and corporate Quality Systems. + Create engineering deliverables including User Requirements, Functional Design Specifications, Network Architectures, Standard Operating Procedures. + Develop test scripts (commissioning/qualification protocols). + Participating in developing software lifecycle plans/road maps. + To develop and implement the Global Automation strategies that will standardize automation group processes and infrastructure. **_ACCOUNTABILITIES_** + Supports technical availability, operation, optimization, maintenance and life cycle management of buildings, systems, production, and infrastructure equipment assigned to automation department. + Supports maintaining a complete and accurate documentation for equipment and systems + Own and develop Automation solutions that are consistent with specific needs of the manufacturing environment. + Drive the Automation roll-out process at the Site level ensuring cost, schedule and technical solution are achieved. + Lead and drive Site working groups to ensure clear action plans with delivery milestones for Automation strategies. + Support harmonization across the network to ensure consistent core solutions are being implemented. + Be aware of technology trends and benchmarks in the industry. Benchmark against peers so that Takeda is inline with industry. + Maintain system data integrity compliance to the current Takeda and industry standards **_DIMENSIONS AND ASPECTS_** **Technical/Functional (Line) Expertise** + Must be able to display in-depth knowledge and expertise in Automation solutions including Siemens, Omron, Mitsubishi (PLC, HMI, SCADA), i-Fix, Wonderware, Inmation (SCADA, Data Management), knowledge of protocols (OPC, Modbus, Ethernet/IP, Profinet, Profibus), SQL databases, scripting language. + Knowledge of GAMP software development lifecycle, ANSI/ISA-88,95,101,105,106 industry standards, 21 CFR Part 11 and Annex 11. + Working knowledge of network architecture technologies including TCP/IP, Routing, Switching, Network IDS/IPS, Active Directory, Domain Integration and Firewalls + Displays strong problem-solving capabilities. + Can display analytical and conceptual thinking. + Has a deep and broad understanding of pharmaceutical manufacturing process, regulatory environment, trends in automation innovation, and financial acumen. + Ability to produce technical documentation to a high standard. + Track record of high performance in relevant reviews. **Interaction** + Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making. + Is able to easily engage with both internal and external stakeholders to drive performance and rollout Automation solutions. + Excellent at knowledge sharing through mentoring and training to lift the average expertise level across the site in their area. + Works with Global Automation to align and implement Automation best practices. + Independent, self-motivated, organised, and able to multi-task in a manufacturing environment **Innovation** + Is capable of identifying new trends in the industry like cloud computing, IoT, AI, etc. + Provides inputs for defining the innovation roadmap in GMS Automation strategies. + Demonstrate ideas for improvements. Contributes to strategic plan for the area. **_REQUIREMENTS:_** + Degree in engineering (M. Sc. / B. Sc.) (automation / robotics / computer science or electrical / process / mechanical / chemical or equivalent) + Experience: min 5 year experience in GMP manufacturing relevant to the specialist area of expertise, including familiarity with principles of data integrity and good documentation practices. + Broad knowledge of Automation solutions and best practice in field of expertise. + High communication skills, analytical mind-set, ability to work under pressure. + GxP/QA knowledge. + Innovative thinking. + Building relationships and teamwork. + Used to working in a complex global / matrix organization. + Can establish and coordinate service contracts with external service providers. **Additional Desired Skills:** + Experience with data analysis. + ANSI/ISA-99,100 standards knowledge + Good understanding of the pharmaceutical industry not limited to technical aspects only. **Locations** Bray, Ireland **Worker Type** Employee **Worker Sub-Type** Regular **Time Type** Full time