Quality Control Biochem
Pubblicato il 15-10-2026 - Altro in Latina
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
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