Thelma Dzeuba

Highly proficient in data review, documentation, analysis, and working in collaboration with cross-functional team to complete tasks.

• CAR-T/LV Associate Tech Specialist – Investigation, Johnson & Johnson Innovative Medicine, 07/01/22, Present, Primary focus in investigations and assess product quality impact., Interview personnel within CAR-T/LV and provide quality insight to complete laboratory investigation reports in Comet., Identify root cause of nonconformance/deviations and provide recommendations for improvement of processes by working cross-functionally with multiple collaborators., Proactively work with team members to implement effective corrective and preventive actions (CAPAs) and to ensure the timely completion of CAPAs within the laboratories.
• CAR-T Scientist – Analytical Development, EUROFINS LANCASTER PSB, 05/01/21, 07/01/22, Perform range of operations, including cGMP and non-GxP clinical sample testing for biopharmaceutical clients using FACS Lyric, as well as 10-color and 2 color flow cytometry methods., Maintain cell culture and prepare cell culture media and buffer as required., Perform peer review/approval of laboratory data., Demonstrate skill in performing method development and transfers and feasibility studies; talent for investigating and troubleshooting method and instrumentation problems and issues., Maintain and monitor reagent inventory and utilization; also promote high quality, safe laboratory environments.
• Senior Laboratory Technician, ROCHE MOLECULAR SYSTEMS, 06/01/19, 05/01/21, Charged with performing range of analytical testing methods using HPLC/UPLC to support development, synthesis, purification, and QC testing for test reagents., Interpreted and followed required SOPs., Performed data entry, analysis, and validation and prepared batch release protocols for BSI and CBER shipment of reagent kits., Prepared final reports for stability protocols and facilitated change requests.
• Laboratory Technician, ROCHE MOLECULAR SYSTEMS, 03/01/16, 06/01/19, Performed QC PCR-based testing of Vials/bulks, components, and finished kits for replenishment and stability, following corresponding SOPs., Conducted laboratory maintenance/cleaning, instrument maintenance, and safety control., Performed tasks in compliance with cGMP, GLP, and OSHA regulations., Managed projects with quality and accuracy, collecting and handling samples, maintaining testing materials, and summarizing experimental results., Ensured completeness, accuracy, consistency, and clarity of project results by reviewing QC documents.
• Biotechnology Research Assistant, RUTGERS UNIVERSITY, 09/01/14, 09/01/15, Cultivating parasitic cells in preparation for drug testing., Preparing media for cell growth., Applying drug treatment as directed., Training new research assistants in proper laboratory procedures.