Quality Control Biochem / Chemistry Testing L1-1

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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