stage 6 mois – assurance qualité système
Core
Maintaining the quality system for external manufacturing and supply of general medicines, supporting site and product transfers, and managing third-party qualification data.
Role type
System Quality Assurance Intern
Builds
Pharmaceutical quality documentation and system maintenance for external manufacturing sites
Domain
Biopharmaceuticals / Regulatory Quality
Deliverable
dashboards & analysis
Required skills
GMP knowledge, regulatory environment knowledge, data management, documentation management, project support, process improvement
Preferred skills
Life sciences, chemistry, or pharmacy background
Responsibilities
Maintain database for third-party, finished product, and active substance qualification; Maintain quality documentation via Sanofi's tool; Support site and product transfer projects; Collaborate on quality agreements with third parties; Support transport validation; Identify process improvement opportunities
