At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function:Supply Chain EngineeringJob Sub Function:Automation EngineeringJob Category:Scientific/TechnologyAll Job Posting Locations:Ringaskiddy, Cork, IrelandJob Description:JOB SUMMARYEstablished and productive individual contributor in a scientific/technology field. Administers automation for modernized and legacy systems, infrastructure, and services. Conducts the planning, design, scheduling and control of Manufacturing Systems projects and process improvements. Contributes to key performance indicator achievements and supports company initiatives.DUTIES & RESPONSIBILITIESInstalls equipment and control systems and helps determine reliability and need for updates.Documents automation project requirements in support o project management, process improvements and maintenance.Conducts routine assessments to determine regulatory compliance and any necessary improvements for regulation conformity.Completes automation deliverables and ensures adherence to expected deadlines.Analyzes complex changes in scope, including provision of necessary information to support claims for time and cost impact.Communicates with subject matter experts regarding workflow and project deliverables internally and externally.Coaches more junior colleagues in techniques, processes, and responsibilities.Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.Responsible for communicating business related issues or opportunities to next management levelResponsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and proceduresPerforms other duties assigned as neededEXPERIENCE AND EDUCATIONESSENTIAL:2 years industry experience in life science or related industryEducation Requirements: Hons Degree in Engineering, Science or a related disciplinePLC ProgrammingExperience in delivery of automation projectsAbility to interpret engineering drawings/specificationsWorking knowledge of Medical Device Quality Systems within a regulated environmentDESIRABLE:Experience in computer system validation.Experience with manufacturing systemsExperience with Database Configuration and MaintenanceExperience with IT NetworksREQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONSHigh attention to detailPro-active approach to workHigh standardsFlexibleExcellent Communication and presentation skillsAnalytical skillsTeam PlayerHighly computer literatePlanner & OrganiserProject ManagementActive ListenerContinuous Improvement focus
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