Technicien Contrôle Qualité – Industrie Pharmaceutique (H/F)

Conduct physicochemical analyses of raw materials, semi-finished, and finished products, including stability studies, adhering to regulatory references (PE, USP) and client Good Manufacturing Practices. Manage full analysis workflows by interpreting results, planning subsequent steps, and documenting outputs within deadlines. Investigate out-of-specification results or anomalies to propose corrective or improvement actions while maintaining laboratory safety and hygiene protocols. Support general laboratory operations to ensure seamless functioning. Requires Bac +2/3 in analytical chemistry with significant HPLC experience in a pharmaceutical GMP environment. Competitive salary with social benefits including family health insurance and transport allowance.