About this role
Pharmaceutical Quality GVP Auditors (Consulting) at Advarra. Location: Tokyo, Tokyo, Japan. Role: conducting audits, preparing reports, evaluating compliance Requirements: 10+ years clinical quality/GVP experience, 5+ years GVP auditing, regulatory knowledge (FDA/EMA), audit program and CAPA experience, bachelor's degree, B2 English and Japanese proficiency. Category: Research and Development Seniority: Senior Level Commitment: Contract Workplace: Remote Languages: English, Japanese