Scientist, QC Compliance, Cell Therapy

Role Lead QC compliance for cell therapy manufacturing, specializing in deviations, investigations, CAPAs, change controls, and process improvements. Responsibilities author and oversee QC deviation reports conduct root cause analysis ensure timely closure of investigations generate KPIs report escalation risks support document revisions mentor colleagues and represent department during inspections Requirements Bachelor's in science/engineering 6+ years in biopharma QC labs, with at least 2 years in investigation strong knowledge of cGMP, quality systems, and technical writing Preferred experience with cell therapy analytical/microbiological testing investigations root cause analysis techniques High-Value focus on cell therapy modalities investigations in GMP manufacturing cross-functional collaboration compliance with global regulatory standards representing QC in inspections WorkSetup not specified, but role involves laboratory and compliance activities. #J-18808-Ljbffr Scorpion Therapeutics