About this role
Auditor I, Clinical Quality Assurance at Iovance Biotherapeutics. Location: United States. Role: supporting audits, implementing procedures, conducting inspections Requirements: BA/BS in life sciences and 1+ year GCP or GMP experience; knowledge of global regulations and guidelines; experience with MasterControl or Veeva; strong project, communication, and critical thinking skills. Category: Quality Assurance Seniority: Entry Level Tools: MasterControl, Veeva, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project Commitment: Full Time Workplace: Remote Languages: English