Cell Therapy Site Production Planner & Scheduler

Bristol Myers Squibb; Leiden; On-site; EUR 90,000 - 130,000; Full time

Benefits offered by this job

Comprehensive benefits

Employee development programs

Job summary

Bristol Myers Squibb Netherlands is seeking a Manager, Site Production Planner and Scheduler to own the master production schedule for Leiden and ensure timely release of orders with available materials and capacity. You will shape scheduling tools, processes, and resource plans across clinical and commercial drug products.

Collaborating with Manufacturing, Quality, and Facility & Engineering, you’ll align with the BMS Global network to ensure end-to-end material availability, from apheresis

Qualifications

• Bachelor or Master’s degree in Supply-Chain, Operations Management, Industrial Engineering, Biology, or similar education.
• 6+ years proven relevant work experience; knowledge of SAP, APO, PPDS, BIO-G or other manufacturing scheduling software is preferred.
• Experience in cGMP biologics manufacturing; cell therapy manufacturing preferred.
• Certification in CPIM, CSCP, and/or CLTD11 is preferred but not required.

Responsibilities

• Create and publish the Site Schedule for Manufacturing Operations and Facility & Engineering teams.
• Mitigate scheduling risks by coordinating with relevant functions.
• Support S&OP process by providing site-level capacities.
• Manage RCCP for assigned products and forecast slot availability.
• Develop scheduling SOPs and drive continuous improvement.

Skills

Leadership

Stakeholder management

Cross-functional teamwork

Communication

Problem solving

Independent work

Education

Bachelor or Master’s degree in Supply-Chain, Operations Management, Industrial Engineering, Biology, or similar education

Tools

SAP

APO

PPDS

BIO-G

Job description

Bristol Myers Squibb Netherlands is seeking a Manager, Site Production Planner and Scheduler to own the master production schedule for Leiden and ensure timely release of orders with available materials and capacity. You will shape scheduling tools, processes, and resource plans across clinical and commercial drug products.

Collaborating with Manufacturing, Quality, and Facility & Engineering, you’ll align with the BMS Global network to ensure end-to-end material availability, from apheresis