960 Qc Analyst jobs in the United Kingdom

QC Analyst required initially on a temporary basis, based in West Yorkshire. Requiring a degree in Chemistry (or similar). Recent Chemistry graduates are encouraged to apply, as well as candidates holding recent, proven industrial experience.

Title: QC Analyst

Location: West Yorkshire

Term: Temporary Contract (Initially, 6 months)

Salary: £24,500 (pro-rata'd for length of contract)

SRG are working with a leading company that develop and manufacture speciality chemicals. They are currently looking to hire a temporary QC Analyst at their site in West Yorkshire, which will predominantly involve supporting in testing of product batches, in-process samples and raw materials. This is a great opportunity for a recent chemistry graduate to gain some valuable industrial laboratory experience with an innovative, market leading chemicals company, with full training given. Alternatively, this role will suit candidates that have proven industrial experience of wet chemistry analysis.

Role / Description

• Carrying out final testing on production batches
• Entering test data in SAP, maintained inspection lots, assigning usage decisions and flagging any out of spec batches
• Compare test data to control limits to identify out of trend batches
• Evaluate customer complaints, carrying out any investigative lab work as required
• Carrying out shelf life extension requests
• Provide testing PT/Quality support to evaluate plant issues/potentially IQ batches
• Conducting testing and supporting ongoing PT projects
• Ensuring testing equipment is in good condition and product calibrations are up to date
• Maintain the lab to 5S standards

Requirements

• A degree in Chemistry (or similar)
• Recent Chemistry graduates are encouraged to apply
• Strong and evidenced problem solving skills.
• High attention to detail
• Ability to efficiently plan, organise and manage own workload

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV to For more information regarding this position or any others, please call Chris on .

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit to view our other vacancies.

Keywords: chemistry, chemist, laboratory technician, laboratory, laboratory technician, analysis, analytical, analysing samples, graduate chemist, graduate, university, wet chemistry, chemicals, industrial, batch samples, raw materials, finished products.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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.

• 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.

About the Role

We’re looking for a QC Analyst to join our Quality Control team! You’ll play a vital role in ensuring our products meet the highest standards of quality and compliance. Working in a fast-paced, GMP-regulated environment, you’ll help deliver safe and effective medicines to patients worldwide

Key Responsibilities

Quality Control Senior Laboratory Analyst (Level 1)

£30,000 + Overtime + Benefits

Full-time, On-site – Berkshire

Monday to Friday, 07:30–15:30 (37.5 hours/week) – Weekend rota supported via overtime

Must have full drivers licence and access to own transport

We’re supporting a leading life sciences organisation in their search for a Senior Quality Control Analyst to join their microbiology lab team based in Berkshire. This is a great opportunity for someone with a solid QC background to contribute to the quality and safety of biological products in a fast-paced, collaborative lab environment. The role offers hands-on testing responsibilities, with added exposure to quality systems and compliance support.

About the Role

As part of the Quality Control team, you’ll focus on microbiological analysis and support production through accurate sampling and timely testing. While your core focus will be lab-based, you’ll also have the opportunity to support QA-related activities such as documentation checks, deviation investigations, and maintaining audit readiness—ideal for someone seeking variety and development in a smaller, adaptable quality team.

You’ll also be part of a structured review process, with clear opportunities to progress to Senior Analyst Level 2 or 3 based on performance.

Key Responsibilities

• Perform microbiological testing and environmental monitoring in line with QC protocols
• Prepare labware, equipment, consumables, and bacterial strains for testing activities
• Support production by initiating sampling routines and antigen preparation
• Review and maintain accurate lab documentation, batch records, and test reports
• Contribute to deviation investigations, change controls, and validations as required
• Help maintain inspection readiness and support internal or external audits
• Lead or support daily planning (PDR) meetings in the QC Supervisor’s absence
• Train and support junior lab team members
• Ensure lab cleanliness, stock control, and biohazard waste disposal

What We’re Looking For

• Degree in Biological Sciences or equivalent lab-based experience
• 1–2 years' experience in a microbiology or quality control laboratory
• Solid understanding of GMP/ISO requirements in a lab environment
• Hands-on lab skills and ability to support documentation and quality processes
• Proactive, organised, and comfortable in a multi-tasking role
• Team player with a flexible approach—especially in a small, dynamic QC/QA team
• Vaccine or biological product experience is a bonus but not essential

Salary & Working Hours

• Salary: £30,000 (with scope for quick progression through senior levels)
• Hours: Monday – Friday, 07:30 – 15:30 (37.5 hours/week)
• Weekend Rota: Occasional weekends with paid overtime

Looking to take the next step in a rewarding QC lab role with real career progression?

If you’re ready to contribute to a mission-driven team in a growing organisation, apply now or get in touch for a confidential chat.

• 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.