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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.

The Automation Engineer will develop and optimize automated QC workflows, troubleshoot systems, and support laboratory operations in a GMP environment.

The Quality Control Analyst will perform analytical testing, including in-process, lot release, and stability testing while ensuring compliance with cGMP guidelines. They will also investigate discrepancies and support equipment validation and documentation for regulatory submissions.

The Automation Engineer will develop and optimize lab automation systems, validate QC workflows, and ensure functionality of automated systems for cell therapy manufacturing.

The Director, Operations Finance will oversee FP&A for the Operations organization, driving financial insights, cost forecasts, and operational efficiencies across manufacturing sites globally.

The Director, Corporate FP&A leads financial planning processes, collaborates with functional leaders, and provides analysis to drive financial performance in a biotechnology setting.