Le poste
03As Production Planner (a), you will be responsible for developing and maintaining manufacturing schedules to support clinical and commercial production activities within a GMP-regulated environment.
01Develop and maintain daily manufacturing production schedules for clinical and commercial programs.
02Support medium- and long-term production planning activities to meet manufacturing demand.
03Manage and coordinate product changeover schedules and timelines.
04Monitor production progress and work closely with manufacturing teams to track completion status and update schedules as needed.
05Ensure accurate planning of resources, capacity, and operational requirements.
06Proactively identify scheduling constraints, risks, and bottlenecks, and propose alternative solutions.
07Support facility readiness activities, including commissioning, qualification/validation (CQV), shutdowns, and changeovers.
08Plan and track maintenance activities (routine and non-routine) to minimize impact on production.
09Collaborate with cross-functional teams including Manufacturing, Materials, Quality, Engineering, Validation, and Plant Management.
10Drive issue resolution to support project and production success.
11Communicate planning, scheduling, and operational updates to stakeholders in a timely manner.
12Report project and scheduling status to management and relevant teams.
13Identify opportunities to improve planning systems and processes and recommend solutions.
