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Seeking a Senior Controls Engineer to lead the design, implementation, and testing of control systems for a cell therapy manufacturing platform. Responsibilities include developing PLC control software, collaborating with cross-functional teams, and validating automation systems. Requires 5+ years of industry experience and expertise in control systems development.
Seeking a Senior Manager, Logistics to manage clinical and commercial vein-to-vein logistics activities for autologous and allogeneic client programs. Responsible for on-time shipment management, vendor performance monitoring, and budget tracking. Key role in coordinating logistics across manufacturing sites and stakeholders to deliver client products. Must ensure compliance with cGMP requirements and regulatory agencies. Multidisciplinary role interfacing with various departments.
The LIMS Developer will design, develop, and implement LIMS solutions, customize workflows for high-throughput cell therapy operations, and collaborate on digital architecture roadmaps. Key responsibilities include capturing software requirements, developing custom scripts, and coordinating with cross-functional teams.
The Logistics Specialist will oversee the shipping and receiving processes, managing logistics and distribution of supplies, ensuring timely delivery of materials, and maintaining compliance with regulations. Responsibilities include cost analysis, inventory accuracy, developing best practices, and improving operational efficiency.
The Automation Scientist will develop and optimize lab automation systems for high-throughput cell therapy manufacturing QC testing, collaborating with various teams to implement automated QC methods, troubleshoot issues, and coordinate validation testing to ensure quality and compliance.
The Associate Scientist in Analytical Development will develop, optimize, and automate various analytical methods for cell therapy. Responsibilities include conducting analytical testing, evaluating new technologies, maintaining documentation, and collaborating with cross-functional teams to support process development and manufacturing.
The Staff Technical Product Manager will understand user needs and workflows for cell therapy manufacturing. They will define product vision, communicate product strategy, synthesize product roadmap, gather and prioritize system requirements, and work closely with cross-functional teams to improve product quality and user satisfaction.
The Manager of Quality Control will oversee routine and non-routine analysis in the GMP laboratory, ensuring compliance with quality standards and regulatory requirements. Responsibilities include managing analytical methods, training personnel, participating in internal audits, and supporting the development and validation of testing methods. This role requires strong collaboration across departments to support manufacturing and quality systems.
The Senior Scientist will develop flow cytometry-based assays for cell therapy products, optimizing protocols and providing analytical support during assay transfer. This role involves data analysis, instrument troubleshooting, and collaboration across teams to enhance testing capabilities and maintain documentation. The candidate will also engage in training and assist in managing laboratory operations.
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