About this role
Senior Documentation Control Specialist at Summit Therapeutics Sub, Inc.. Location: Palo Alto or Menlo Park or Princeton or Miami. Role: uploading documents, archiving documents, maintaining compliance Requirements: 5+ years in biotech/pharma QA, documentation control, QMS; GLP/GCP and 21 CFR knowledge; strong communication; highly organized; MS Office proficiency. Category: Quality Assurance Seniority: Senior Level Tools: MS Office, Quality Management System, QMS Commitment: Full Time Workplace: Onsite Languages: English