QC Analyst

About the role

Join SGS as a QC Analyst in a GMP‑compliant pharmaceutical laboratory. You will perform raw material and drug substance testing, primarily using GC and HPLC, while supporting a multicultural, global team.

Key responsibilities

• Carry out analytical testing according to validated procedures and regulatory requirements.
• Maintain and calibrate laboratory equipment on schedule.
• Manage inventory of consumables and reagents required for analysis.
• Enter and verify data in the LIMS, review results generated by peers, and close out batch analyses.
• Document findings, write SOPs, methods and reports, and communicate status in team meetings.
• Lead investigations and deviations, ensuring audit readiness and safety compliance.
• Support KPI achievement in areas such as productivity, on‑time testing and training.

Required profile

• Experienced QC Analyst with a background in pharmaceutical testing.
• Familiarity with GMP standards and ability to work in a regulated environment.
• Willingness to train junior analysts and pursue continuous development.

Required skills

• Gas Chromatography (GC)
• High‑Performance Liquid Chromatography (HPLC)
• LIMS data entry and management
• Laboratory equipment calibration and maintenance
• Inventory management for analytical supplies
• SOP and analytical method documentation
• GMP compliance

What we offer

• Opportunity to work with a world‑leading testing and certification company.
• Access to continuous training and professional development.
• Collaborative, multicultural work environment.