20 ott - Bardi
Sanofi
In 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. * Sampling and handling of Raw Material, intermediate and finished products as per SOPs * Managing sample storage and external testing coordination * Performing analysis of RMs, intermediates, stability samples, and finished goods per specs * Ensuring cGLP in laboratory activities and audit readiness * Documentation: raw data, ATR records, logbooks,
calibration and qualification documents * Reviewing and revising test procedures; raising deviations and CAPAs via Qualipso * Result recording and data review in SAP ATHENA; instrument qualification * Support on digitalization and simplification of QC activities; address OOS/OOT deviations * Carry out instrument calibration, preventive maintenance, and method validation * HSE adherence and training to maintain zero risk and ISO 14001 compliance * MSc in Chemistry * 3 years of experience in quality control or related field * Basic knowledge of HPLC and instrumental analysis * Raw material testing * Finished product testing * SOP adherence and regulatory documentation Quality Control Biochem / Chemistry Testing L1-1 mantova, lombardia, it #J-18808-Ljbffr
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