About this role
Specialist I, Quality Control Compliance at Iovance Biotherapeutics. Location: Philadelphia, Pennsylvania, United States. Role: managing documentation, maintaining lifecycle, creating certificates Requirements: Bachelor's in biological sciences, 3+ years cGMP QC experience in biopharma, LIMS experience, detail-oriented, strong communication and analytical skills, able to manage multiple priorities. Category: Research and Development (R&D) Seniority: Mid Level Tools: LIMS Commitment: Full Time Workplace: Onsite Languages: English