Quality Control Biochemist: HPLC & Instrumentation

Sanofi

Lodi

On-site

EUR 6,500 - 9,200

Full time

2 days ago
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Job summary

Sanofi in Goa seeks a qualified QC Analyst to support testing of raw materials, intermediates and finished products. You will perform instrumental analyses and ensure cGLP, with focus on documentation and audit readiness.

The role involves data review, instrument qualification, and supporting digitalization of QC activities, while maintaining safety and ISO 14001 compliance in a fast-paced pharmaceutical environment.

Qualifications

  • Requires MSc in Chemistry and at least 3 years of experience in quality control or related field.
  • Excellent knowledge of instrumental analysis and regulatory documentation is essential.
  • Candidates should have basic knowledge of HPLC and instrumental analysis and strong attention to SOPs.

Responsibilities

  • Sampling and handling of raw materials, intermediates and finished products per SOPs.
  • Managing sample storage and external testing coordination.
  • Performing analyses of RMs, intermediates, stability samples, and finished goods per specs.
  • Ensuring cGLP in laboratory activities and audit readiness.
  • Instrumental analyses (HPLC, GC, UV-Vis, IR, Raman, Dissolution).
  • Documentation: raw data, logbooks, calibration and qualification records.
  • Reviewing and revising test procedures; raising deviations and CAPAs via Qualipso.
  • Result recording and data review in SAP ATHENA; instrument qualification.

Skills

Quality control experience
Instrumental analysis
Documentation and SOP adherence

Education

MSc in Chemistry

Tools

HPLC
UV-Vis
IR
Raman
Dissolution

Job description

Sanofi in Goa seeks a qualified QC Analyst to support testing of raw materials, intermediates and finished products. You will perform instrumental analyses and ensure cGLP, with focus on documentation and audit readiness.

The role involves data review, instrument qualification, and supporting digitalization of QC activities, while maintaining safety and ISO 14001 compliance in a fast-paced pharmaceutical environment.

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