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The IT Systems Engineer will support and optimize IT infrastructure, automate tasks, resolve issues, maintain security, and collaborate cross-functionally.

Oversee daily operations of the Quality Control lab, ensuring compliance with regulations, leading investigations, and maintaining a high standard of inspection readiness.

The Associate Director leads supply chain planning and procurement, optimizing manufacturing systems, ensuring process compliance, and developing strategies for capacity planning. They also mentor teams and drive data-driven decision-making.

The Associate Director of Market Development will engage with Key Opinion Leaders (KOLs), develop brand strategies, manage marketing budgets, and ensure cross-functional collaboration for the commercial launch of cell therapies.

Support lifecycle management of commercial cell therapy manufacturing processes: monitor/process metrics, investigate trends and events, lead process improvements and validations, author change controls/protocols, troubleshoot equipment/material issues, and manage MSAT projects including new materials, packaging, and cold chain considerations.

The Analyst, Enterprise Data Integration ensures data integrity across Orca Bio's systems, manages data integration, performs data validation, and supports cross-functional reporting needs. The role involves executing commercial data tasks as part of transitioning to a centralized data warehouse.

The Senior Director of FP&A will lead financial planning, forecasting, and reporting, enhance FP&A processes, and partner with various functions for budgeting and strategic planning.

The Manager, Commercial Manufacturing oversees GMP operations, manages staff, ensures compliance with regulations, fosters continuous improvement, and promotes safety in cell therapy production.

The Specialist, Training develops and delivers training programs for GMP operations, ensures compliance with SOPs and safety protocols, and assesses trainee competencies.

The Director of Commercial Manufacturing leads GMP operations, ensuring timely, compliant delivery of patient-specific therapies while driving continuous improvement and quality standards.