Strategic Master Scheduler - GMP Manufacturing

A leading US-based cell therapy firm in Princeton is seeking a Master Scheduler to develop and maintain the comprehensive Master Production Schedule. The role involves coordinating across Manufacturing, Quality Control, and Process Development teams to ensure an optimal flow of materials, resources, and quality activities. Candidates should have over 8 years of experience in production planning or related roles in GMP environments, along with a Bachelor’s degree in relevant fields.

The company fosters a collaborative culture and focuses on reliable product delivery in a strong regulatory framework.
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