The Specialist, QC Analytical, performs routine and non-routine analytical testing to support cGMP lot release and stability of cell therapy products. The role executes approved methods, including flow cytometry, ELISA, PCR, automated cell counting, and other cell-based assays, while maintaining high quality, data integrity, and accurate documentation. The Specialist participates in laboratory investigations and collaborates with the QC team and cross-functional partners to meet testing timelines and ensure compliant operations. This is an on-site laboratory position in Rockville, Maryland, scheduled for four 10-hour day shifts per week, Wednesday through Saturday.
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Job Type
Full-time
Career Level
Mid Level