268 Quality Control Analyst jobs in the United Kingdom

Quality Control Analyst

Dewsbury, Yorkshire and the Humber Network Scientific Recruitment

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Job Description

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.

This advertiser has chosen not to accept applicants from your region.

Quality Control Analyst

Liverpool, North West SRG

Posted 2 days ago

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Job Description

  • 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
This advertiser has chosen not to accept applicants from your region.

Quality Control Analyst

Dewsbury, Yorkshire and the Humber Network Scientific Recruitment

Posted today

Job Viewed

Tap Again To Close

Job Description

Job Description

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.

This advertiser has chosen not to accept applicants from your region.

Quality Control Analyst - Pharmaceutical

CV1 2GN Coventry, West Midlands £35000 Annually WhatJobs

Posted 8 days ago

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Job Description

full-time
Our client, a prominent pharmaceutical manufacturer, is seeking a meticulous and dedicated Quality Control Analyst to join their state-of-the-art facility in Coventry, West Midlands, UK . This crucial role involves performing a wide range of analytical tests to ensure the quality, safety, and efficacy of pharmaceutical products throughout the manufacturing process. The successful candidate will work with advanced analytical instrumentation and contribute to maintaining the highest standards of quality compliance. This is an excellent opportunity for an individual with a strong background in analytical chemistry and a commitment to pharmaceutical quality.

Key Responsibilities:
  • 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.
Qualifications:
  • 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.
This on-site role offers a competitive salary, comprehensive benefits, and opportunities for professional development within a leading pharmaceutical organisation. Contribute to the quality and safety of essential medicines.
This advertiser has chosen not to accept applicants from your region.

Pharmaceutical Quality Control Analyst

EH1 2HB Edinburgh, Scotland £40000 Annually WhatJobs

Posted 11 days ago

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Job Description

full-time
Our client, a prominent pharmaceutical company in **Edinburgh**, is seeking a meticulous and analytical Pharmaceutical Quality Control Analyst to join their vital laboratory team. This role is critical in ensuring the safety, efficacy, and quality of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment such as HPLC, GC, and UV-Vis spectrophotometers. Adherence to strict Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) guidelines is paramount. The ideal candidate will possess a strong scientific background, ideally in chemistry, biochemistry, or a related field, with a Bachelor's degree or higher. Proven experience in a pharmaceutical QC laboratory setting is essential. You will be skilled in method validation, instrument calibration, and data interpretation. Accurate record-keeping and detailed report writing are integral to this position. The ability to work independently and as part of a team, managing multiple tasks efficiently and meeting deadlines, is crucial. This role demands exceptional attention to detail, a commitment to scientific integrity, and a proactive approach to problem-solving. You will contribute to the continuous improvement of quality control processes and participate in regulatory audits. The successful applicant will be dedicated to upholding the highest standards of quality and compliance within the pharmaceutical industry. This is an excellent opportunity to advance your career in pharmaceutical quality assurance.Location: This role is based at our client's facility in **Edinburgh**, Scotland, UK.
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Pharmaceutical Quality Control Analyst

MK9 2EU Milton Keynes, South East £30000 Annually WhatJobs

Posted 11 days ago

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Job Description

full-time
Our client, a reputable pharmaceutical company in Milton Keynes, Buckinghamshire, UK , is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst. This role is crucial in ensuring that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements. The successful candidate will perform a variety of laboratory tests and analyses on raw materials, in-process samples, and finished products using sophisticated analytical instrumentation. Responsibilities include executing validated analytical methods, meticulously documenting all experimental procedures and results, and adhering to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will be responsible for operating and maintaining laboratory equipment, troubleshooting analytical issues, and participating in method validation and transfer activities. A key aspect of this role involves contributing to deviation investigations and ensuring that any quality issues are addressed promptly and effectively. A Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific discipline is required. Prior experience in a pharmaceutical QC laboratory setting, with hands-on experience in techniques such as HPLC, GC, spectroscopy (UV-Vis, IR), and wet chemistry, is highly desirable. Strong understanding of pharmacopoeial standards (e.g., USP, EP) and regulatory guidelines (e.g., MHRA, FDA) is essential. Excellent organisational skills, attention to detail, and the ability to manage multiple tasks in a fast-paced environment are critical. This role offers a hybrid working arrangement, allowing for a balance between on-site laboratory work and remote administrative tasks. Our client provides a supportive work environment with opportunities for continuous learning and professional development in the pharmaceutical quality assurance field.
This advertiser has chosen not to accept applicants from your region.

Pharmaceutical Quality Control Analyst

LE3 1JQ Leicester, East Midlands £35000 Annually WhatJobs

Posted 13 days ago

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Job Description

full-time
A leading pharmaceutical manufacturer in **Leicester, Leicestershire, UK**, is seeking a meticulous and highly organized Pharmaceutical Quality Control Analyst to join their dedicated QA/QC team. This role is integral to ensuring the quality, safety, and efficacy of pharmaceutical products by performing a range of analytical tests on raw materials, in-process samples, and finished goods. You will operate sophisticated laboratory equipment, interpret test results, and maintain accurate records in compliance with Good Manufacturing Practices (GMP) and regulatory guidelines. The ideal candidate will possess strong analytical skills, a keen attention to detail, and a solid understanding of pharmaceutical quality control principles.

Key Responsibilities:
  • 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).

Qualifications:
  • 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.

This is an excellent opportunity for a dedicated scientist to contribute to the development and manufacturing of life-saving medicines within a reputable pharmaceutical company.
This advertiser has chosen not to accept applicants from your region.
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Pharmaceutical Quality Control Analyst

WV1 3LF Wolverhampton, West Midlands £28000 Annually WhatJobs

Posted 16 days ago

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Job Description

full-time
Our client, a reputable pharmaceutical company, is looking for a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their laboratory team in **Wolverhampton, West Midlands, UK**. This on-site role is critical for ensuring the quality and safety of pharmaceutical products through rigorous testing and analysis.

Key Responsibilities:
  • 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.
Essential Qualifications and Experience:
  • 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.
This is an excellent opportunity for a dedicated QC Analyst to contribute to the pharmaceutical industry in a role that directly impacts product quality and patient safety.
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Senior Pharmaceutical Quality Control Analyst

CV1 1DT Coventry, West Midlands £40000 Annually WhatJobs

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Job Description

full-time
Our client, a prominent player in the pharmaceutical industry, is seeking an experienced Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art laboratory in Coventry, West Midlands, UK . This pivotal role involves conducting rigorous analytical testing on raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with regulatory standards and internal specifications. The successful candidate will be responsible for performing a variety of analytical techniques, including HPLC, GC, spectroscopy, and wet chemistry methods. You will also be involved in method development and validation, instrument calibration and maintenance, data interpretation and review, and the investigation of out-of-specification (OOS) results. This position requires a meticulous approach to documentation, adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), and a strong understanding of pharmaceutical quality systems. Collaboration with R&D, manufacturing, and regulatory affairs departments is also a key aspect of this role. The ideal candidate will possess a BSc or MSc in Chemistry, Pharmaceutical Science, or a related field, with several years of relevant experience in a pharmaceutical QC environment. Excellent analytical skills, problem-solving abilities, and strong written and verbal communication are essential. Opportunities for professional growth and development within a supportive and innovative team.
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Senior Pharmaceutical Quality Control Analyst

EH4 2BZ Edinburgh, Scotland £45000 Annually WhatJobs

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Job Description

full-time
Our client is seeking a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art laboratory facilities. This role is integral to ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of analytical tests, developing and validating test methods, and maintaining comprehensive documentation in compliance with regulatory standards (e.g., GMP, ICH). The ideal candidate will possess a strong background in analytical chemistry, experience with various analytical techniques, and a keen eye for detail.

Key Responsibilities:
  • 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.

Required Qualifications:
  • 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.

This is an excellent opportunity for a skilled QC professional to advance their career within a leading pharmaceutical company. The role is based in **Edinburgh, Scotland, UK**, and requires attendance at the specified location.
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