About this role
T2609 Clinical Development Quality Manager (contractor until end of May 2027) at Debiopharm. Location: Lausanne, Vaud, Switzerland. Role: ensuring compliance, monitoring kqis, managing audits Requirements: University degree in sciences, 4+ years clinical pharmaceutical/biotech experience with ≥3 years in clinical quality management, GCP/CFR21 knowledge, audit and vendor oversight experience, KQI monitoring, CAPA and SOP experience. Category: Research and Development (R&D) Seniority: Mid Level Commitment: Contract Workplace: Onsite Languages: English