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The Consumable Quality Engineer will lead the testing and validation of consumables, ensuring compliance with ISO 10993 and USP Class VI standards. Responsibilities include developing qualification plans, executing a range of tests, coordinating with external labs, analyzing test results, and collaborating across departments.

The Associate Scientist will support cell therapy manufacturing by designing and executing experiments aimed at process development and improvement. Responsibilities include maintaining cell lines, generating process documentation, addressing project challenges, and performing laboratory activities. The role requires strong technical writing skills and knowledge of cell therapy methods.

Seeking a Senior Analytical Transfer Specialist to lead analytical method transfers, evaluation, and support for cell therapy QC operations. Responsibilities include authoring procedures, contributing to regulatory submissions, and providing technical leadership. Requires a Bachelor's degree and 4+ years of experience in biologics/gene therapy with knowledge of QC principles and relevant analytical methods.

The Automation Engineer will support the deployment and optimization of automated QC testing workflows, validate methods for sample preparation and analysis, monitor system performance, conduct validation testing, and develop troubleshooting methodologies. They will work collaboratively with cross-functional teams and contribute to system documentation and training.

The Senior Manager of Operational Technology will oversee technical operations and infrastructure in an industrial and cell therapy lab, ensuring 24x7 operational support. Responsibilities include managing OT systems, developing implementation plans, ensuring compliance with security best practices, troubleshooting production issues, and delivering training for OT staff, while interacting with senior leadership and business functions to align priorities.

Seeking a VP, CMC Process Sciences to oversee establishment and execution of CMC development plans for cell and gene therapy products. Responsible for providing CMC leadership, collaborating with stakeholders, and driving effective communication and coordination across functional groups.

Seeking a VP of Operations to oversee the launch and operations of a cGMP cell therapy manufacturing facility. Responsibilities include leading a team, ensuring compliant operations, collaborating with key stakeholders, and driving continuous improvements and efficiencies.