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Develop and refine system requirements while leading projects in cell therapy systems design. Mentor team members and ensure streamlined project development by integrating customer requirements with technical specifications.

The Office Manager will oversee daily office operations, manage events, collaborate with teams, track budgets, and maintain a professional environment, requiring strong multitasking and organizational skills.

The Senior Systems Integration Engineer will lead system characterization, integration, troubleshooting, and continuous improvement of cell therapy manufacturing systems, collaborating with various teams and driving tasks to completion.

Lead the development of control systems for cell therapy manufacturing by designing, implementing, testing hardware controls, and collaborating across teams.

The Process Engineer will support automated cell therapy manufacturing processes, collaborating across teams to design, validate, and optimize efficient workflows and documentation.

The QC LIMS Administrator supports the Laboratory Information Management System in the QC department, managing data related to cell therapy and ensuring compliance within a GMP environment.

The Quality Control Analyst conducts QC testing, prepares reports, investigates discrepancies, and supports regulatory compliance for cell therapy products.

The Principal SAP Technical Architect will be responsible for the design, development, and support of SAP systems in a GMP environment, engaging in ABAP programming, Fiori development, and integration with middleware platforms while collaborating with cross-functional teams.

Lead the technical transfer of a mechanical system to a contract manufacturer, while managing design and ensuring manufacturability. Requires 15+ years experience in mechanical engineering.

The Project Manager will lead SAP implementation projects in GMP-regulated environments, overseeing project lifecycles, compliance, and cross-functional collaboration within biotech operations.