h3Overview /h3pIn 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. /ph3Responsabilità /h3ulliSampling and handling of Raw Material, intermediate and finished products as per SOPs /liliManaging sample storage and external testing coordination /liliPerforming analysis of RMs, intermediates, stability samples, and finished goods per specs /liliEnsuring cGLP in laboratory activities and audit readiness /liliInstrumental analysis (HPLC, GC, UV-Vis, IR, Raman, Dissolution, etc.) /liliDocumentation: raw data, ATR records, logbooks,



calibration and qualification documents /liliReviewing and revising test procedures; raising deviations and CAPAs via Qualipso /liliResult recording and data review in SAP ATHENA; instrument qualification /liliSupport on digitalization and simplification of QC activities; address OOS/OOT deviations /liliCarry out instrument calibration, preventive maintenance, and method validation /liliHSE adherence and training to maintain zero risk and ISO 14001 compliance /li /ulh3Requisiti fondamentali /h3ulliMSc in Chemistry /lili3 years of experience in quality control or related field /liliBasic knowledge of HPLC and instrumental analysis /liliLanguages: English, Hindi, Marathi /li /ululliRaw material testing /liliFinished product testing /liliInstrument handling (HPLC, UV-Vis, IR, Raman, Dissolution, etc.) /liliSOP adherence and regulatory documentation /li /ul #J-18808-Ljbffr

📌 Quality Control Biochem (Teramo)
🏢 Sanofi
📍 Teramo