Quality Control Biochem / Chemistry Testing L1-1

Sanofi; Chieti; On-site; EUR 5,500 - 8,800; Full time

Job summary

Sanofi in Goa seeks a QC Analyst to support quality control testing of raw materials, intermediates and finished products, ensuring compliant release and stability data. You will perform instrumental analyses (HPLC, GC, UV-Vis, IR, Raman) and maintain rigorous documentation, audit readiness and cGMP compliance in a fast- paced pharmaceutical setting.

Applicant should hold an MSc in Chemistry with 3 years of QC experience and knowledge of HPLC.

Qualifications

• MSc in Chemistry with 3 years of QC experience.
• Basic knowledge of HPLC and instrumental analysis.
• Fluent in English, Hindi and Marathi.

Responsibilities

• Sampling and handling of raw material, intermediates and finished products.
• Managing sample storage and external testing coordination.
• Performing analysis of RMs, intermediates, stability samples, and finished goods.
• Ensuring cGLP and audit readiness.
• Instrumental analyses (HPLC, GC, UV-Vis, IR, Raman, Dissolution).
• Documenting raw data, ATR records, logbooks, calibration and qualification documents.
• Reviewing and revising test procedures; raising deviations and CAPAs.
• Result recording and data review in SAP ATHENA; instrument qualification.
• Support on calibration, preventive maintenance and method validation.
• HSE adherence and ISO 14001 compliance.

Skills

HPLC

Instrumental analysis

Quality control

SOP adherence

Education

MSc in Chemistry

Tools

SAP ATHENA

Job description

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