Pharma QC Analyst: HPLC & Stability Testing

Cypartners; Worthing; On-site; GBP 26,000 - 38,000; Full time

Job summary

CY Partners are recruiting for a QC Analyst on behalf of a leading global pharmaceutical manufacturer based in Worthing. This role supports the release of life-changing medicines and works within a high-performing Quality Control team.

You will perform physical and chemical testing of oral products, support stability studies, ensure GMP/GLP compliance, and contribute to timely analytical data delivery alongside QA and Production.

Qualifications

• HNC, Degree, or equivalent qualification in Chemistry or a related scientific discipline.
• Understanding of laboratory analytical techniques.
• Ability to work effectively in a fast-paced manufacturing environment.
• GMP/GLP knowledge is desirable.

Responsibilities

• Perform testing of production and stability samples to meet QC lead-time targets.
• Conduct qualitative and quantitative analysis of antibiotic powders and solid dose formulations.
• Utilise analytical techniques including HPLC, Karl Fischer, dissolution testing.
• Calibrate, maintain, and troubleshoot laboratory equipment.
• Document analytical results in accordance with GMP and QC procedures.
• Investigate OOS results and communicate findings with QC leadership, QA, Production.
• Review and verify analytical data generated by colleagues.
• Support laboratory safety standards, GLP, and training compliance.
• Collaborate with analysts, team leaders, QA, and manufacturing to ensure timely data delivery.
• Take a lead role on specific analytical techniques where required.

Skills

Analytical techniques

Quality control teamwork

Education

HNC in Chemistry

Degree in Chemistry

Tools

HPLC

Karl Fischer Titration

Dissolution Testing

Job description

CY Partners are recruiting for a QC Analyst on behalf of a leading global pharmaceutical manufacturer based in Worthing. This role supports the release of life-changing medicines and works within a high-performing Quality Control team.

You will perform physical and chemical testing of oral products, support stability studies, ensure GMP/GLP compliance, and contribute to timely analytical data delivery alongside QA and Production.