Quality Control (QC) Analyst in Cowbridge

Energy Jobline ZR; Cowbridge; On-site; GBP 27,000; Full time

Job summary

A recruitment agency is seeking a Quality Control Analyst in Cowbridge, UK. The successful candidate will conduct laboratory tests to ensure product compliance with regulations. A Bachelor's degree in a scientific discipline and skills in analytical instrumentation are essential. This 6-month fixed-term role offers a salary of £27,000 per annum with a 4 on, 4 off schedule.

Qualifications

• Bachelor's degree required in relevant scientific discipline.
• Familiarity with analytical instrumentation necessary.
• Strong understanding of GLP, GMP, or ISO standards.

Responsibilities

• Conduct laboratory tests and analyses per standards.
• Maintain detailed records in compliance with GLP.
• Participate in method development and continuous improvement.

Skills

Attention to detail

Time management

Organisational skills

Problem-solving skills

Strong communication abilities

Education

Bachelor's degree in a scientific discipline

Tools

HPLC

GC

Microsoft Office

LIMS

Job description

Energy Jobline is the largest and fastest growing global Energy Job Board and Energy Hub. We have an audience reach of over 7 million energy professionals, 400,000+ monthly advertised global energy and engineering jobs, and work with the leading energy companies worldwide.

We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.

Job Description

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 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 Confident Employer and is committed to helping find great work opportunities for great people.

If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.