General Responsibilities. Contribute to the development, optimization, and execution of analytical assays and process methodologies in support of Castle Creekâs autologous cell therapy program. This role is primarily laboratory-based and requires strong technical skills, meticulous documentation, and clear communication of experimental results. Responsibilities. Execute laboratory experiments involving primary cell culture, bioreactor operations,...
General Responsibilities. Responsible for performing a variety of tasks in support of the daily production of sterile cell therapy products. Tasks are predominately performed within a cleanroom environment under current Good Manufacturing Practices (cGMP) conditions. Responsibilities. Proficient in aseptic processing including media exchanges, vessel passaging, harvest & cryopreservation of cells as required by the daily production schedule. Abil...
General Responsibilities. This individual leads the internal and external manufacturing, supply chain, and facilities and engineering functions that support the cGMP production of preclinical, clinical, and late-stage commercial products. The VP of Manufacturing develops and executes the clinical manufacturing plan aligned with clinical supply forecasts ensuring effective capacity utilization and resource management and consistent performance to ...
Multiple positions available: Cell Culture, ELISA, EM/Micro, Flow Cytometry, PCR. General Responsibilities. Perform testing in support of product manufacturing, employing manual and automated analytical equipment. Provide direct support of Quality Control analytical processes, test procedures, qualifications, validations, assay troubleshooting, equipment upkeep, logbook review, and inventory control. Essential Requirements. Must have direct subje...
