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Job Description
Key Role Overview:
The Planning Supervisor is responsible for ensuring efficient production scheduling, material availability, and capacity planning, while also overseeing new product planning from R&D to market launch and variation batches. This includes coordinating with the Registration Department and R&D Department to align with production capabilities.
Job Accountabilities:
A. Production Planning & Scheduling
- Develop and manage weekly and monthly production schedules based on demand forecasts, machine capacity, and raw material availability.
- Ensure balanced production loading across different machines to avoid overutilization or bottlenecks.
- Coordinate with Manufacturing, Engineering, and QA to ensure planned batches align with equipment availability and validation schedules.
- Monitor First Pass Yield & Batch Rejections to adjust planning and minimize rework.
B. Material Planning & Procurement Coordination
- Ensure raw materials and packaging materials are available before production to prevent stoppages.
- Collaborate with Procurement to optimize supplier lead times and prevent overstocking or shortages.
- Work on MRP (Material Requirements Planning) system for real-time tracking of material availability.
- Work on ROP (Re-Order Point) Ensure optimal inventory levels by continuously monitoring stock movement, calculating re-order points, and triggering purchase or production orders.
- Work with Quality Control (QC) to ensure incoming raw materials are released on time for production and release of finished products for market.
C. Capacity Planning & Machine Utilization
- Monitor machine efficiency and downtime trends to adjust scheduling accordingly.
- Align production plans with maintenance schedules to ensure minimal disruption.
- Support investment planning for new equipment based on capacity limitations and projected demand increases.
D. New Product Planning, Launch Coordination and variation batches
- Work closely with R&D, Regulatory Affairs, and Production to ensure smooth transition from development to commercial production.
- Track new product timelines with R&D Department and align production planning with regulatory approvals.
- Ensure production capacity is available for pilot batches, stability studies, and validation runs before full-scale launch.
- Monitor progress on CTD dossier submission, regulatory approvals, and bioequivalence studies with the Registration Department.
- Follow up variation batches with R&D, Registration, production and quality assurance departments to ensure it's achievement.
E. Cross-Functional Coordination & Issue Resolution
- Act as the main communication link between Production, R&D, Registration, Procurement, and QA to resolve scheduling conflicts.
- Work closely with Engineering & Maintenance to integrate preventive maintenance into the production plan.
- Participate in weekly New Product Development (NPD) meetings to track project milestones.
- Ensure real-time updates of production status to avoid last-minute schedule changes.
Job Requirements
- Bachelor’s degree in science.
- 3-5 years of experience in Production Planning in the pharmaceutical industry.
- Strong knowledge of MRP/ERP systems, capacity planning, and production scheduling.
- Experience in New Product Development coordination and regulatory timelines.
- Excellent analytical, problem-solving, and communication skills to coordinate across multiple departments.
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