CDI - Coordinateur Qualification / validation (F/H)
Core
Coordinateur Qualification / validation responsible for writing qualification documentation, risk analyses, and validation plans for pharmaceutical manufacturing processes.
Role type
Quality Assurance Coordinator (Validation & Qualification)
Builds
Pharmaceutical injectable products (liquids and lyophilized) and active pharmaceutical ingredients
Domain
Pharmaceutical manufacturing / Industrial subcontracting
Required skills
GMP compliance, risk assessment, validation planning, non-conformance management, technical writing, regulatory documentation
Responsibilities
Write qualification documentation (FAT/SAT, QI, QO, QP protocols and reports), conduct risk analyses and traceability matrix reviews, execute and validate qualification operations, participate in validation plan and report development, update qualification procedures
Seniority
Mid-level, hands-on IC
