QC Analyst

Cypartners; Worthing; On-site; GBP 80,000 - 100,000; Full time

Job summary

A leading recruitment agency has a contract opportunity for a QC Analyst in Worthing, UK. The role involves physical and chemical testing, ensuring compliance with GMP regulations, and performing analyses on pharmaceutical products. Ideal candidates will have a solid background in quality testing and hands-on experience with HPLC. This is an excellent chance to advance in your QC career within the pharmaceutical industry.

Qualifications

• Experience in a GMP-regulated lab.
• Hands-on expertise with HPLC.
• Detail-oriented and methodical.

Responsibilities

• Perform testing of production and stability samples.
• Analyse formulations using HPLC and other techniques.
• Maintain analytical instruments and ensure compliance.

Skills

HPLC

Pharmaceutical analysis

GMP regulations

Analytical chemistry

Documentation

Data reporting

Education

HNC, HND, BSc or equivalent in Chemistry

Job description

QC Analyst
Location: Worthing, West Sussex
Salary: £15.64 p/h
Employment Type: 6 Month Contract

CY Partners have an exciting contract opportunity for aQC Analyst with a background in pharmaceutical analysis. Do you have hands-on expertise with HPLC and other analytical techniques? If so, this could be a fantastic opportunity to further your career within a dynamic and fast-paced QC environment.

This is a key role within the Quality function, supporting the release and stability testing of sterile and non-sterile products.

Key Responsibilities:

• Perform physical and chemical testing of production and stability samples, meeting turnaround times and compliance standards.
• Analyse solid dose and antibiotic formulations using HPLC, Karl Fischer, dissolution, and other wet chemistry techniques.
• Calibrate, verify, and maintain analytical instruments and systems.
• Review and verify analytical results, ensuring data integrity and compliance with GMP/GLP.
• Support investigations into Out-of-Specification (OOS) results, working cross-functionally where needed.
• Contribute to the validation of analytical methods and equipment.

About You:

You’ll ideally bring a strong background in pharmaceutical quality testing, with sound knowledge of GMP regulations and analytical chemistry.

Requirements:

• HNC, HND, BSc or equivalent in Chemistry or a related scientific discipline.
• Proven experience in a GMP-regulated lab, with hands-on experience using HPLC.
• Strong documentation and data reporting skills.
• Detail-oriented, methodical, and safety-conscious.
• Able to communicate clearly and work effectively as part of a multidisciplinary team.
• A proactive, flexible approach to working in a fast-moving manufacturing environment.

Whether you’re looking to build on your experience or take the next step in your QC career, this is a great opportunity to make a meaningful impact within the pharmaceutical industry.