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This role involves supporting cell therapy manufacturing processes, leading technology transfers, developing automation, ensuring GMP compliance, and collaborating across departments.

Lead the execution of enterprise AI strategy by operationalizing AI across business systems, focusing on adoption, governance, and measurable ROI in a fast-paced environment.

The Principal Enterprise Data Architect will design and operationalize a data platform, integrating various systems while leading data governance and AI readiness efforts.

The position leads method transfer, validation, and optimization of cell therapy analytical methods while collaborating across departments to ensure compliance and support product development.

The Director of Quality Compliance will lead compliance activities, manage quality systems, ensure GMP adherence, and oversee inspections and audits.

The HR Business Partner serves as the on-site HR resource, providing employee support and managing HR processes in a manufacturing environment while partnering with leadership to ensure compliance and improve HR practices.

The Manufacturing Supervisor oversees cGMP operations and manages the production of cell therapy products, ensuring compliance, team development, and process optimization.

The Manufacturing Support Services Specialist supports manufacturing and warehouse operations, performing routine procedures in a GMP environment, training new associates, and ensuring compliance with SOPs and safety policies.

The Senior Director of IDMO Site Quality leads QA/QC operations for cell therapy manufacturing, ensuring compliance with cGMP while fostering collaboration across departments and stakeholders for successful product outcomes.

Cellares seeks a Senior Scientist in Process Development to execute and analyze experiments for cell therapy, interface cross-functionally, and mentor junior staff.