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Scorpion Therapeutics is seeking a CAR T Production Planning and Scheduling Specialist to oversee inventory verification, regulatory reporting, and material management in biopharma manufacturing at our Summit, New Jersey site. You will coordinate supplier delivery schedules, maintain accurate records, and contribute to GMP-compliant processes.
Familiarity with regulatory standards and CAR T workflows is highly valued.
CAR T Production Planning and Scheduling Specialist responsible for inventory verification, regulatory compliance reporting, and material management activities in biopharma manufacturing.
Relevant degree, experience in biopharma production, inventory management, or supply chain, with familiarity in regulatory standards and compliance documentation.
Experience with CAR T therapies or cell/gene modalities, knowledge of GMP regulations, and proficiency in material traceability systems.
Focus on biopharma manufacturing, inventory oversight, regulatory reporting, and supplier coordination within a biotech or pharmaceutical setting.
Not explicitly stated, but likely on-site based on manufacturing context.