268 Quality Control Analyst jobs in the United Kingdom

• Job Title: QC Specialist – Biosafety
• Location: Speke, Liverpool.
• Contract: until end of July 2026 initially
• Rate: £15.25 (inclusive of shift uplift)
• Shift : 4 on 4 off, 7am-7pm

SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst (Biosafety) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate with some experience to further their career.

Main responsibilities:

• Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations.
• Performing routine QC testing
• Documenting laboratory results in an accurate and timely manner.
• Complying with GMP regulatory requirements at all times.

Key requirements:

• Experience of working to GMP/pharmaceutical regulatory requirements is desirable.
• Biological background either from university degree or relevant work in the field
• Computer skills, excel, word, outlook

Preferrable

• Experience within cell cultures and/or assay testing.
• LIMS and SAP

Are you looking for some further experience in Pharmaceutical QC? Do you have prior experience with GC & HPLC in a cGMP environment?

A Global Pharmaceutical Manufacturer are seeking a QC Analyst to join the team at their site in Kirklees. This is a 6 month FTC and would be ideal if you are immediately available and looking to add to your existing experience in Pharmaceutical QC.

Role Overview

• Full Time , 6 month Fixed term Contract. Day Shifts. £27,000pa.
• Analysis of Raw Materials and Finished Products to SOPs.
• Utilise analytical equipment , predominantly HPLC & GC.
• Interpretation and checking of Analytical Data.
• Monitoring, Calibration and occasional basic troubleshooting/maintenance of instruments and analytical equipment.
• Preparation of all relevant documentation in line with applicable standards.

Requirements

• Prior working experience in a cGMP environment using HPLC and GC is essential.
• Degree or equivalent in relevant scientific discipline (or equivalent working experience) is essential.
• Ability to work independently in time pressured environment.
• Excellent communication skills and attention to detail.

In return

This 6 month FTC is an excellent opportunity to add some additional experience to your CV, working alongside industry leaders in a well renowned pharmaceutical organisation.

For more information, please contact Louis Williams

If this QC Analyst job is not quite right for you, but you’re interested in similar opportunities, please take a look at our other Jobs in the Pharmaceutical Sector. Network Scientific is a multi-award-winning recruitment agency dedicated to connecting top talent with opportunities across the scientific and technical sectors. We specialise in temporary, permanent, and contract placements, and pride ourselves on being an ethical and knowledgeable consultancy with a strong focus on candidate care.

Please note that all applicants for this role should be able to prove that they are legally entitled to work in the country specified. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

• Conduct routine and non-routine analytical testing on raw materials, in-process samples, and finished products.
• Perform tests using various laboratory techniques, including HPLC, GC, UV-Vis spectroscopy, and titrations.
• Prepare reagents, standards, and samples for analysis.
• Operate and maintain analytical instruments, ensuring calibration and performance.
• Accurately record test results and maintain laboratory documentation in compliance with GMP.
• Investigate out-of-specification (OOS) results and participate in root cause analysis.
• Prepare certificates of analysis and analytical reports.
• Ensure laboratory safety procedures are followed at all times.
• Participate in method validation and transfer activities.
• Collaborate with production, quality assurance, and R&D teams.
• Stay updated with current Good Manufacturing Practices (GMP) and relevant pharmacopoeial standards.

• Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related science discipline.
• Minimum of 2-3 years of experience in a Quality Control laboratory, preferably within the pharmaceutical industry.
• Hands-on experience with HPLC and other common analytical techniques.
• Knowledge of GMP principles and regulatory requirements.
• Proficiency in laboratory data recording and documentation.
• Strong attention to detail and accuracy.
• Good organisational and time management skills.
• Ability to work effectively both independently and as part of a team.
• Excellent problem-solving skills.
• Good written and verbal communication skills.

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using various techniques (e.g., HPLC, GC, UV-Vis spectroscopy, titration).
• Operate and maintain laboratory equipment, ensuring it is calibrated and in good working order.
• Prepare reagents, solutions, and standards accurately.
• Interpret test results and compare them against established specifications.
• Document all laboratory activities, results, and deviations meticulously in accordance with GMP guidelines.
• Investigate out-of-specification (OOS) results and assist in root cause analysis.
• Participate in method validation and transfer activities.
• Maintain a clean and organized laboratory environment.
• Adhere to all safety protocols and procedures.
• Contribute to continuous improvement initiatives within the QC department.
• Assist in the preparation of quality control reports and regulatory submissions.
• Ensure compliance with all relevant regulatory requirements (e.g., MHRA, FDA).

• Bachelor's degree in Chemistry, Pharmaceutical Science, Biology, or a related scientific discipline.
• Proven experience working in a pharmaceutical Quality Control laboratory environment.
• Hands-on experience with analytical instrumentation such as HPLC, GC, dissolution testers, and spectrophotometers.
• Strong understanding of GMP, regulatory guidelines, and quality systems in the pharmaceutical industry.
• Excellent analytical, problem-solving, and critical thinking skills.
• Proficiency in scientific documentation and record-keeping.
• Attention to detail and commitment to accuracy.
• Good communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Experience with LIMS (Laboratory Information Management System) is a plus.

• Perform a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products according to established Standard Operating Procedures (SOPs) and pharmacopoeial methods.
• Utilise analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometry, and dissolution apparatus.
• Prepare reagents, standards, and solutions required for testing.
• Accurately record and document all test results, maintaining detailed batch records and laboratory notebooks.
• Evaluate test results against specifications and report any deviations or out-of-specification (OOS) results promptly.
• Calibrate and maintain laboratory equipment, ensuring it is in good working order.
• Assist in the validation and verification of analytical methods.
• Participate in internal quality audits and assist with regulatory inspections.
• Ensure compliance with Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and other relevant regulatory guidelines.
• Contribute to the investigation of quality issues and OOS results.
• Maintain a safe and clean working environment within the laboratory.
• Support inventory management of laboratory consumables and reagents.
• Engage in continuous professional development to stay updated with analytical techniques and regulatory requirements.

• BSc in Chemistry, Pharmaceutical Science, or a related scientific discipline.
• Previous experience working in a Quality Control laboratory, preferably within the pharmaceutical industry.
• Proficiency in using common analytical laboratory equipment (e.g., HPLC, GC).
• Strong understanding of GMP and regulatory requirements in the pharmaceutical sector.
• Excellent attention to detail and accuracy in data recording and reporting.
• Good understanding of analytical principles and methodologies.
• Ability to follow complex procedures and SOPs accurately.
• Strong organisational and time-management skills.
• Effective communication skills, both written and verbal.
• Ability to work effectively both independently and as part of a team.
• Proficiency in Microsoft Office Suite.

• Perform routine and non-routine analytical testing of raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, Karl Fischer titration, and dissolution testing.
• Develop, validate, and transfer analytical methods according to regulatory guidelines.
• Analyze and interpret test results, ensuring accuracy and completeness.
• Prepare Certificates of Analysis (CoA) and other quality documentation.
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Maintain laboratory equipment and instrumentation, including calibration and qualification.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant quality standards.
• Participate in internal and external audits.
• Train and mentor junior QC analysts.
• Contribute to continuous improvement initiatives within the QC department.

• Bachelors or Master's degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
• Minimum of 5 years of experience in pharmaceutical Quality Control.
• Extensive hands-on experience with HPLC, GC, and other relevant analytical instrumentation.
• Thorough understanding of GMP/ICH guidelines and pharmaceutical quality systems.
• Proficiency in method development and validation.
• Strong analytical, problem-solving, and investigative skills.
• Excellent documentation and communication skills.
• Ability to work independently and as part of a team in a laboratory environment.
• Familiarity with laboratory information management systems (LIMS) is a plus.