OverviewIn this role, you will support quality control testing of raw materials, intermediates, and finished products to ensure compliant release and stability data. You will work within Sampling & Analysis to uphold cGLP, perform instrumental analyses (HPLC, GC, UV-Vis, etc.), and maintain rigorous documentation and audit readiness. You'll contribute to digitalization efforts and instrument qualification while ensuring safety and regulatory compliance in a fast-paced pharmaceutical environment. This is an opportunity to help Sanofi deliver life-changing medicines at scale from Goa.ResponsabilitàSampling and handling of Raw Material, intermediate and finished products as per SOPsManaging sample storage and external testing coordinationPerforming analysis of RMs, intermediates, stability samples, and finished goods per specsEnsuring cGLP in laboratory activities and audit readinessInstrumental analysis (HPLC, GC, UV-Vis, IR, Raman, Dissolution, etc.)Documentation: raw data,



ATR records, logbooks, calibration and qualification documentsReviewing and revising test procedures; raising deviations and CAPAs via QualipsoResult recording and data review in SAP ATHENA; instrument qualificationSupport on digitalization and simplification of QC activities; address OOS/OOT deviationsCarry out instrument calibration, preventive maintenance, and method validationHSE adherence and training to maintain zero risk and ISO 14001 complianceRequisiti fondamentaliMSc in Chemistry3 years of experience in quality control or related fieldBasic knowledge of HPLC and instrumental analysisLanguages: English, Hindi, MarathiRaw material testingFinished product testingInstrument handling (HPLC, UV-Vis, IR, Raman, Dissolution, etc.)SOP adherence and regulatory documentation

📌 Quality Control Biochem / Chemistry Testing-1 (Casagiove)
🏢 Sanofi
📍 Casagiove