Supply Chain Planner

The Company: A global biotechnology and pharmaceutical organization focused on developing, manufacturing, and supplying innovative medicines to patients worldwide. The Breda site supports medicines for close to 100 markets and operates in a highly regulated, complex international supply chain environment.

About the Role: The Senior Associate Supply Chain Detailed Scheduler is responsible for creating and maintaining detailed production schedules for packaging operations. The role ensures reliable product supply by coordinating production capacity, orders, materials, and operational priorities. You will work closely with manufacturing, quality, warehouse, and supply chain teams while improving planning stability, operational performance, and planning processes.

Responsibilities: Manage short term production planning for packaging lines; create detailed production plans and manage production orders; ensure timely product delivery and stable supply to patients; support product introductions, transitions, launches, and phase out activities; identify and resolve operational flow stoppers; measure weekly and monthly planning KPIs including Master Production Schedule stability; define and follow up improvement actions with relevant stakeholders; participate in and facilitate daily operational meetings; coordinate activities between supply chain, manufacturing, quality, and warehouse teams; lead weekly capacity meetings and align realistic production plans; improve planning processes through standardization, simplification, and automation; lead continuous improvement initiatives and root cause analysis activities; support stable operations while working according to GMP and GDP requirements.

Requirements: Bachelor or Masters degree in supply chain, business, science, engineering, or a related discipline; experience within supply chain planning; strong analytical and problem solving skills; strong communication and stakeholder management abilities; ability to collaborate effectively across different departments; experience with root cause analysis and continuous improvement; interest in process standardization and automation; experience with Tableau, Smartsheet, Databricks, or RPA is preferred; experience within a regulated GMP environment is beneficial; ability to work on site for a minimum of three days per week.