Job Title: Production Operator (O2 Level)Location: Site-basedShift Pattern: 24/7 Shift RoleAbout the RoleAn exciting opportunity has arisen for a Production Operator to join a high-performing manufacturing team operating in a regulated, cleanroom environment. As part of an empowered Integrated Process Team (IPT), you will play a key role in ensuring the safe, compliant, and reliable manufacture of products while supporting continuous improvement across operations.Key ResponsibilitiesOperate and monitor production processes and equipment using MES/DCS and PLC-based systems to achieve target outputs and optimal equipment uptimeWork with equipment including parts washers, autoclaves, CIP/SIP systems, vial washers, dehydrogenation tunnels, debaggers, and filling machinesPerform cleanroom cleaning, housekeeping, and materials management in line with cGMP requirementsMaintain full certification and proficiency across assigned equipment, processes, and tasksProactively manage equipment flow, including labeling, inventory control, and tracking sterile/clean hold times using MES and Kanban systemsCarry out preventative maintenance, basic troubleshooting, and repairs where qualifiedSupport the development and rollout of operational procedures and training materialsParticipate in investigations, root cause analysis, change controls, Kaizen events, and improvement projectsIdentify and escalate issues related to safety, quality, people, or delivery in a timely mannerEngage actively in Tier 1 processes at shift start and end, communicating clearly with team membersTake ownership of personal safety and contribute to a strong safety and compliance cultureSupport training and development of colleaguesComplete at least one improvement project or operational excellence initiative per yearEducation & ExperienceLeaving Certificate or equivalent (required)Apprenticeship, Certificate, or Diploma in a related discipline (preferred)Previous experience in a cleanroom or sterile manufacturing environment is advantageousSkills & CompetenciesStrong understanding of cleanroom behaviours, sterile practices, and ALCOA principlesFamiliarity with cGMP and regulated manufacturing environmentsEagerness to learn, develop, and take feedback on boardFlexible and adaptable to shift work and role versatilityStrong teamwork, communication, and problem-solving skillsExperience with downtime logging systems, batch documentation, and basic batch review is beneficialComfortable supporting validation, technical engineering, and maintenance activities as requiredAdditional RequirementsWillingness to obtain and maintain all required safety certifications (e.g. Manual Handling, Material Transfer, Pallet Truck)Active engagement in safety systems and continuous improvement initiatives