Senior QC Analyst

QCS Staffing Ltd; Dublin; On-site; EUR 65,000 - 75,000; Full time

Job summary

QCS Staffing Ltd is recruiting a Senior QC Analyst for an 11-month contract in Ireland, near Dublin, to support a global life sciences client. The role focuses on ensuring robust QC testing through HPLC, UPLC, GC and Capillary Electrophoresis, and to help drive GMP-compliant laboratory operations.

You will contribute to start-up activities, qualification, and readiness in a biologics manufacturing environment, investigate deviations, OOS/OOT, and implement corrective actions to maintain

Qualifications

• Extensive experience in a pharmaceutical or biotechnology QC laboratory environment.
• Hands-on experience with analytical techniques including HPLC, UPLC, GC, and Capillary Electrophoresis.
• Good understanding of GMP/cGMP requirements, laboratory compliance, and regulatory standards.
• Experience investigating laboratory deviations, OOS/OOT results, and troubleshooting analytical issues.

Responsibilities

• Perform QC laboratory testing using HPLC, UPLC, GC, Capillary Electrophoresis, and other analytical techniques.
• Support laboratory start-up, qualification, and operational readiness activities within a biologics manufacturing environment.
• Investigate laboratory deviations, OOS/OOT results, and analytical issues while implementing effective corrective actions.
• Ensure all testing, documentation, and laboratory activities are completed in accordance with GMP and regulatory requirements.

Skills

HPLC

UPLC

GC

Capillary Electrophoresis

GMP/cGMP compliance

Deviations investigations

Job description

Senior QC Analyst – Ireland – Initial 11-Month Contract – Life Sciences

Our client is a global leader in pharmaceutical innovation, specialising in the development and manufacture of cutting-edge drugs. As they continue to grow, they’re seeking an experienced Senior QC Analyst to support their dynamic team and drive forward groundbreaking projects near Dublin.

What you’ll deliver:

• Perform QC laboratory testing using HPLC, UPLC, GC, Capillary Electrophoresis, and other analytical techniques.
• Support laboratory start-up, qualification, and operational readiness activities within a biologics manufacturing environment.
• Investigate laboratory deviations, OOS/OOT results, and analytical issues while implementing effective corrective actions.
• Ensure all testing, documentation, and laboratory activities are completed in accordance with GMP and regulatory requirements.

What you’ll need:

• Extensive experience in a pharmaceutical or biotechnology QC laboratory environment.
• Strong hands-on experience with analytical techniques including HPLC, UPLC, GC, and Capillary Electrophoresis.
• Good understanding of GMP/cGMP requirements, laboratory compliance, and regulatory standards.
• Experience investigating laboratory deviations, OOS/OOT results, and troubleshooting analytical issues.