Quality Control Biochem / Chemistry Testing L1-1

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.

Verifichi qui sotto se possiede i requisiti per questa opportunità e, in tal caso, invii la sua candidatura il prima possibile.

• 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 xysqume
• 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

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