QC Analyst

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.

• 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.

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

• 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.

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

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.

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 with in 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.