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 ManufacturingJob Sub Function: Manufacturing AssemblyJob Category: ProfessionalAll Job Posting Locations: Ringaskiddy, Cork, IrelandJob Description:ROLE TITLE: Graduate Manufacturing Process SpecialistSTART DATE: September 2026LOCATION: Cork, IrelandABOUT THE JOHNSON & JOHNSON GRADUATE PROGRAMME:The Graduate Programme is a collaborative programme across the Johnson & Johnson Campus Ireland Sites. It is aimed at high potential individuals who, when given the right tools, are empowered to proactively take responsibility, effect change and make a positive contribution to their teams and the business.THE SUCCESSFUL CANDIDATE WILL HAVE THE OPPORTUNITY TO:Develop relevant technical skills within their area of expertise.Experience cross functional exposure both on site and within Campus Ireland.Participate in regular one to ones and feedback to support your on-going development.Engage in personal development and effectiveness training.Develop influencing & communication skills.Gain Project Management experience.Learn new and innovative technologies.Gain exposure to Senior Management Team.Participate in continuous professional development program with a recognised qualification.POSITION SUMMARY:Reporting to Operations Manager, this position is responsible for representing operations on capital project teams and supporting first line troubleshooting of the day-to-day activities within Operations - These activities include but are not confined to:ORGANISATIONAL INTERFACES:Interface at (Team Leader, Manager and Director level) with all site departments, Operations and Maintenance.Contact with Engineering, Quality, Logistics, OTS, Validation and Training departments.Contact with other J&J Innovative Medicine sites. Be conscious of internal customers to Manufacturing department and be cognoscente of their requirements.ROLE & RESPONSIBILITIESMonitoring and troubleshooting of the manufacturing process and equipment issues and process optimization.Monitoring and reporting of process performance using statistical process controlTroubleshooting of DCS (e.g Delta V) and PLC control systems.Investigating and resolving issues raised within the Manufacturing Department.Participate in/ Lead Cross Functional teams when required.Support of Commissioning and Qualification activities.Preparation and updating of Batch Records, Procedures and Work Instructions.Provide process and equipment related training as required within the Manufacturing Department.Completion of assigned tasks to support manufacture of quality biomedicines in accordance with cGMP and EHS requirements.Completion of all documentation in compliance with site procedures and GDP.Lead, support and participate in commissioning and qualification activities both current and future projects (and annual re-qualification activities.Prioritize and schedule activities to support business needs and to meet requirements of Master Production Schedule.Support ongoing studies by Validation, OTS and other support functions.EDUCATION & EXPERIENCEEssential:Minimum bachelor’s level degree in either Microbiology, Biochemistry, Pharmacy, Biotechnology, Science, Engineering or equivalent.A recent graduate (2025 or due to graduate in 2026)Experience of Microsoft Word, Excel and Outlook.Experience of SAP, LIM’s and/or other business systems.6-Sigma/Kepner-Tregoe or similar problem solving/decision making methodology trainingExcellent interpersonal skills.Ability to operate as part of a team is critical.Customer focus.Innovative.Mechanical/Technical aptitude.Excellent communication skills both written and verbal.Attention to detail.Desirable:Knowledge/experience in:A GMP regulated environment.Cell culture or purification processes.Project / New equipment installation.Process engineeringDCS (e.g. Delta V), SCADA and PLC systems
