Quality Control (QC) Analyst

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

Salary: £27,000p.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.

Main 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.

Blue Arrow is proud to be a Disability Confident Employer and is committed to helping find great work opportunities for great people