Quality Control Biochem / Chemistry Testing L1-1

Sanofi; La Spezia; On-site; EUR 5,600 - 8,400; Full time

Job summary

Sanofi in Goa, India seeks a Quality Control Analyst to support testing of raw materials, intermediates, and finished products, ensuring cGLP and audit readiness.

You will perform analyses (HPLC, GC, UV-Vis), document data, and contribute to digitalization and instrument qualification while maintaining safety and regulatory compliance.

The role requires MSc in Chemistry and about 3 years of QC experience; hands-on testing of RM, intermediates, stability samples, and finished goods.

Qualifications

• MSc in Chemistry required.
• 3 years of experience in quality control or related field.
• Basic knowledge of HPLC and instrumental analysis.
• Experience with RM/intermediate/finished product testing.
• Follows SOPs and regulatory documentation.

Responsibilities

• 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
• HSE adherence and training to maintain zero risk and ISO 14001 compliance

Skills

Quality control experience

HPLC

Instrumental analysis

Documentation practices

SOP adherence

Education

MSc in Chemistry

Tools

Qualipso

SAP ATHENA

Job description

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.

• 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
• 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