Iovance Biotherapeutics in Philadelphia is seeking a Quality Control Compliance Specialist I to manage QC documentation, data filing and storage, and to oversee the QC lot lifecycle using LIMS, issuing CoA and CoT to support product releases. The role requires a Bachelor’s degree in biological sciences or related field, at least 3 years in a cGMP QC environment, and excellent attention to detail with strong written and verbal communication; ability to collaborate with cross-functional teams #J-18808-Ljbffr
Quality Control Compliance Specialist I • New York, NY, United States
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