Quality Control Chemist: HPLC/GC Analyst, cGLP

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

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.