Production Scheduler RK9512 Contract 12 months Cork Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. The Operations Support Specialist - Production Scheduler is responsible for overseeing and directing biotech production planning, execution, and control. This role involves translating the master production schedule, project plans, and maintenance requirements into detailed day-to-day schedules Duties: Convert the Master Production Schedule (MPS) into detailed day-to-day production schedules. Optimize production schedules based on MPS, operational demands, and available capacity. Assist in the development of medium-term plans to support scenario analysis, conflict analysis, and production schedule business decisions. Provide planning support to the operations team for all operations planning-related aspects. Assist the Operations Team Lead in coordinating operations activities and responding to changes in demand. Act as the main point of contact for all functional areas to gather critical planning information required for updating and progressing operations plans (e.g., validation, maintenance, engineering, etc.). Promote an environment conducive to planning improvements aligned with site strategies, ensure MPS alignment, and incorporate project feedback into production plans. Facilitate daily operations team meetings and weekly supply review meetings. Conduct monthly resource forecasting in collaboration with Operations Team Leads. Communicate the production plan across operations areas, identifying any production or material constraints that may affect progress. Work with operations and planning groups to resolve constraints. Respond to changes in demand/schedule by analyzing updated plans and highlighting areas of risk or schedule conflict to the operations manager. Collect and disseminate data required for monthly reporting. Generate and present daily, weekly, and monthly reports and metrics as necessary. Experience and Education: Third-level qualification, preferably in a science-related field. 2-3 years of experience in (bio) pharmaceutical manufacturing. Relevant qualification in Supply Chain Management (e.g., APICS, IIPMM) advantageous. Lean/Continuous Improvement qualifications advantageous If interested in this posting please feel free to contact Rachel Kent on or for further information. Skills: GMP Supply Chain Production Planning
