Technical Learning Specialist I, GMP Training Administration

Role: GMP Training Administration Specialist I at Iovance’s Cell Therapy Center, supporting technical learning programs and LMS operations. Responsibilities: manage training documentation review, generate training reports, maintain qualification records, support onboarding, troubleshoot LMS issues, assist in curriculum development, and contribute to training process improvements. Requirements: Bachelor’s degree (Life Sciences preferred), 2+ years in pharmaceutical or biopharma GMP training/documentation, familiarity with document change management, FDA quality systems, and LMS platforms (MasterControl preferred); strong attention to detail, communication, and organizational skills. HighValue: biopharma GMP environment, cell therapy manufacturing, training compliance, LMS administration, Good Documentation Practices, data integrity, cross-functional teamwork. WorkSetup: onsite Philadelphia; physical ability to perform office and lab activities.