Quality Control (QC) Analyst

Blue Arrow; Cowbridge; On-site; GBP 27,000; Full time

Job summary

A recruitment agency is seeking a Quality Control Analyst for a 6-month contract in Llantrisant. The candidate will perform laboratory tests, monitor production processes, and ensure compliance with regulatory standards. Requirements include a Bachelor's degree in a scientific field and familiarity with analytical techniques. The role offers a £27,000 annual salary with a unique 4 on, 4 off shift pattern.

Qualifications

• Bachelor's degree in chemistry, Biochemistry, Pharmaceutical Science, or related field.
• Familiarity with analytical instrumentation and software.
• Strong understanding of GLP, GMP, or ISO standards.

Responsibilities

• Conduct laboratory tests and analyses for product quality.
• Calibrate and maintain laboratory equipment.
• Support audits and ensure compliance with safety regulations.

Skills

Analytical techniques

Attention to detail

Problem-solving

Communication skills

Organizational skills

Education

Bachelor's degree in a scientific discipline

Tools

HPLC

GC

UV-Vis

FTIR

Job description

Overview

Blue Arrow is recruiting a Quality Control (QC) Analyst to join our client's team based in the Llantrisant area.

Salary: £27,000 p.a.

Hours: 4 days on, 4 days off, 10-hour shifts from 07:00 to 18:00

Contract: 6 month fixed term contract

Role Overview

As a QC Analyst, you will be responsible for conducting a variety of laboratory tests and analyses to ensure our products meet regulatory standards and client specifications. You will play a key role in monitoring production processes, identifying deviations, and implementing corrective actions to maintain the integrity and safety of our products.

Responsibilities

• Perform routine and non-routine analyses of raw materials, in-process samples, and finished products using established analytical techniques (e.g., FPLC, UV-Vis, FTIR, titration, wet chemistry).
• Interpret and report analytical results accurately, maintaining detailed and organised records in compliance with Good Laboratory Practices (GLP) and company SOPs.
• Calibrate, operate, and maintain laboratory equipment, ensuring all instruments are functioning optimally and maintaining calibration logs as required.
• Participate in method development, method validation, and continuous improvement initiatives to optimise laboratory performance.
• Conduct investigations into non-conforming results and work collaboratively to determine root causes and implement effective corrective actions.
• Assist in the preparation and review of technical documents such as SOPs, test methods, specifications, and validation protocols.
• Support internal and external audits by providing necessary documentation, data, and explanations regarding laboratory practices and results.
• Ensure all laboratory activities are conducted in accordance with health, safety, and environmental regulations.
• Collaborate with cross-functional teams, including production, quality assurance, and research and development, to resolve quality issues and drive continuous improvement.
• Stay current with advances in analytical techniques, regulatory requirements, and industry best practices.

Requirements

• Bachelor's degree in chemistry, Biochemistry, Pharmaceutical Science, Microbiology, Food Science, or a related scientific discipline.
• Familiarity with analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR) and associated software.
• Strong understanding of GLP, GMP, or ISO standards as applicable to the industry.
• Excellent attention to detail, time management, and organisational skills.
• Strong communication abilities, both written and verbal, and ability to convey technical information clearly.
• Problem-solving skills and an investigative mindset.
• Ability to work independently as well as collaboratively in a fast-paced, team-oriented environment.
• Proficient in using standard office and laboratory software (e.g., Microsoft Office, LIMS).

Desirable Skills

• Experience with method development and validation.
• Knowledge of statistical analysis and data interpretation.
• Familiarity with regulatory submissions and documentation (e.g., MHRA, FDA, EMA).
• Previous experience in root cause analysis and CAPA (Corrective and Preventive Action) processes.
• Additional language skills are an advantage.

If you feel you would be suitable for the above role, please submit your CV for immediate response.

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