Quality Control Biochem / Chemistry Testing L1-1

Sanofi; Friuli-Venezia Giulia; On-site; EUR 5,200 - 8,000; Full time

Job summary

Sanofi is seeking a quality control professional to support testing of raw materials, intermediates, and finished products to ensure compliant release data. You will perform analyses (HPLC, GC, UV-Vis) within Sampling & Analysis, uphold cGLP, and maintain rigorous documentation and audit readiness in a fast-paced pharmaceutical setting.

The role includes instrument qualification, data review, CAPAs, and contributing to digitalization efforts while ensuring safety and regulatory compliance.

Qualifications

• 3 years of experience in quality control or related field.
• MSc in Chemistry is required.

Responsibilities

• Sampling and handling of Raw Material, intermediate and finished products 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

cGLP compliance

Documentation

Audit readiness

Digitalization

Safety training

Education

MSc in Chemistry

Tools

HPLC

GC

UV-Vis

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