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Lead and stabilize GMP-critical enterprise and manufacturing systems (ERP, MES, QMS, PLM, LIMS), ensure data integrity and traceability, drive integrations, governance, and validation, partner with Manufacturing/Quality/Finance, and provide hands-on leadership to make systems audit-ready and scalable for commercial manufacturing.

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.

Lead and support IT/OT operations in a biotech manufacturing lab, ensuring system reliability and compliance with industry regulations.

The Senior Electrical Engineer will lead electrical design for automation equipment, ensuring compliance and managing design documentation. Responsibilities include collaborating with teams, conduct prototyping, and driving design reviews based on industry standards.

The Director of Enterprise Programs leads client programs in process development, managing teams, overseeing tech transfer, ensuring compliance, and optimizing manufacturing processes for cell therapies.

The Senior Director, Supply Chain leads and develops the Supply Chain organization, implementing strategies for efficiency in materials management, logistics, and production planning within a biotech environment.

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