Work as part of the Health Sciences Immunologic Monitoring and Cellular Products Laboratory (IMCPL) team. Perform advanced laboratory testing and processing. Manufacture cellular therapy products for patient treatment Utilize cutting-edge techniques and advanced instrumentation. Author SOPs and qualify, validate processes and platforms for process development, process control, and product release.Perform specialized. Quality Control tests related to CGT product development and clinical studies. This includes testing for identity, purity, composition, integrity, safety, activity, stability, viability, and potency assays. Collect background information for testing/experiments/production; initiate paperwork, perform test set-up, work area, and equipment. Calculate and analyze assay/test results and quality control information. Investigate abnormal results in accordance with established protocols. Implement all quality controls to ensure assay and process validity; adhere to departmental safety standards in responsibly handling, processing, and testing specimens and materials. Follow cGMP (current good manufacturing practices) guidelines in the production of cellular products. Be self-driven, sincere, thorough, and have an eye for details

Performs a variety of independent and complex laboratory work and experiments. Analyzes and interprets data, compiles results, and prepares reports. Maintains inventory, ordering, and logs. Writes manuscripts and grant proposals and prepares data visualizations.

Work as part of the Health Sciences Immunologic Monitoring and Cellular Products Laboratory (IMCPL) team. Perform advanced laboratory testing and processing. Manufacture cellular therapy products for patient treatment Utilize cutting-edge techniques and advanced instrumentation. Author SOPs and qualify, validate processes and platforms for process development, process control, and product release.Perform specialized. Quality Control tests related to CGT product development and clinical studies. This includes testing for identity, purity, composition, integrity, safety, activity, stability, viability, and potency assays. Collect background information for testing/experiments/production; initiate paperwork, perform test set-up, work area, and equipment. Calculate and analyze assay/test results and quality control information. Investigate abnormal results in accordance with established protocols. Implement all quality controls to ensure assay and process validity; adhere to departmental safety standards in responsibly handling, processing, and testing specimens and materials. Follow cGMP (current good manufacturing practices) guidelines in the production of cellular products. Be self-driven, sincere, thorough, and have an eye for details

Bending, lifting to put away supplies. Walking between building. Sitting and standing for long periods at the bench. Reading small font.

The University of Pittsburgh is an equal opportunity employer / disability / veteran.