QC Analyst

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

QC Analyst

Location: Worthing, West Sussex
Sector: Pharmaceutical Manufacturing | Quality Control

CY Partners are currently recruiting for a QC Analyst on behalf of a leading global pharmaceutical manufacturer based in Worthing. This is an excellent opportunity to join a high-performing Quality Control team supporting the release of life-changing pharmaceutical products to market.

Working within a collaborative team you will be responsible for performing physical and chemical testing of oral pharmaceutical products, supporting stability studies, and ensuring all analytical work is completed in compliance with GMP, GLP, and internal quality standards.

Key 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 a range of analytical techniques including:
  • HPLC
  • Karl Fischer Titration
  • Dissolution Testing
  • Other pharmaceutical analytical methods
• Calibrate, maintain, and troubleshoot laboratory equipment.
• Accurately document analytical results in accordance with GMP and Quality Control procedures.
• Investigate Out of Specification (OOS) results and communicate findings with QC leadership, QA, Production, and Qualified Persons as required.
• Review and verify analytical data generated by colleagues.
• Support the maintenance of laboratory safety standards, Good Laboratory Practice (GLP), and training compliance.
• Collaborate closely with analysts, team leaders, QA, and manufacturing teams to ensure timely delivery of analytical data and reports.
• Take a lead role on specific analytical techniques where required.

About You

We are looking for a motivated and detail-oriented laboratory professional.

Essential Requirements

• 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.

Desirable Experience

• Pharmaceutical Quality Control experience.
• GMP and/or GLP knowledge.
• Experience with HPLC, dissolution testing, and Karl Fischer analysis.
• Experience investigating OOS results.

About the Site

The Worthing manufacturing facility specialises in the production of antibiotic medicines. Candidates should consider this when applying and must disclose any pre-existing penicillin allergy as part of the application process.

Why Apply?

This is an opportunity to join a globally recognised pharmaceutical organisation that develops and manufactures medicines used by millions of people worldwide. You'll work within a supportive QC team, gain exposure to a wide range of analytical techniques, and contribute directly to maintaining the quality and safety of pharmaceutical products.