Overview 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. Responsabilità
* 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
* Instrumental analysis (HPLC, GC, UV-Vis, IR, Raman, Dissolution, etc.)
* 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 Requisiti fondamentali
* MSc in Chemistry
* 3 years of experience in quality control or related field
* Basic knowledge of HPLC and instrumental analysis
* Languages: English, Hindi, Marathi
* Raw material testing
* Finished product testing
* Instrument handling (HPLC, UV-Vis, IR, Raman, Dissolution, etc.)
* SOP adherence and regulatory documentation

📌 Quality Control Biochem (Biella)
🏢 Sanofi
📍 Biella