h3Overview /h3 pIn 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. /p h3Responsabilità /h3 ul liSampling and handling of Raw Material, intermediate and finished products as per SOPs /li liManaging sample storage and external testing coordination /li liPerforming analysis of RMs, intermediates, stability samples, and finished goods per specs /li liEnsuring cGLP in laboratory activities and audit readiness /li liInstrumental analysis (HPLC, GC, UV-Vis, IR, Raman, Dissolution, etc.) /li liDocumentation: raw data, ATR records, logbooks,



calibration and qualification documents /li liReviewing and revising test procedures; raising deviations and CAPAs via Qualipso /li liResult recording and data review in SAP ATHENA; instrument qualification /li liSupport on digitalization and simplification of QC activities; address OOS/OOT deviations /li liCarry out instrument calibration, preventive maintenance, and method validation /li liHSE adherence and training to maintain zero risk and ISO 14001 compliance /li /ul h3Requisiti fondamentali /h3 ul liMSc in Chemistry /li li3 years of experience in quality control or related field /li liBasic knowledge of HPLC and instrumental analysis /li liLanguages: English, Hindi, Marathi /li /ul ul liRaw material testing /li liFinished product testing /li liInstrument handling (HPLC, UV-Vis, IR, Raman, Dissolution, etc.) /li liSOP adherence and regulatory documentation /li /ul #J-18808-Ljbffr

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