By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda'sPrivacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job DescriptionJOB PURPOSE: SME in Manufacturing Control Systems, Operational Technology, Machine Automation and DigitalizationAct 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.LocationsBray, Ireland
Worker TypeEmployee
Worker Sub-TypeRegular
Time TypeFull time
#J-18808-Ljbffr