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Quality Control Laboratory Analyst GMP / GLP Kent

Opportunity:

Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you!

Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards.

Testing techniques may include, but is not limited to, routine particle size analysis (Malvern Mastersizers, Sympatec), cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation (including particle size and cleanability assessments), DSC, Light microscopy, SEM, Moisture content (Karl Fisher), method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses.

You will also get involved in CAPA s, deviations and document control.

The hours of work are:

• Early shift 6am - 2pm Monday-Friday for 3 weeks then it changes to
• Late shift 1.30pm - 10pm Monday-Thursday, 1.30pm - 7pm Friday for 3 weeks then it changes to
• Night shift 9pm - 7am Monday - Thursday for 3 weeks then back to the early shift.

This is a 12 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour.

Skills:

To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills:

• Degree or equivalent in a scientific subject.
• Experience in wet chemistry / analytical techniques ideally within the pharmaceutical or related industry.
• Need to be clean-shaven due to working in clean rooms.
• No make up, false eye lashes and nail varnish due to working in clean rooms.

How to Apply:

To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.

If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

For a list of our current vacancies, please visit the Quality Start website.

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.

Quality Start are acting as a specialist recruitment consultancy for this role.

We are seeking a motivated and detail-oriented Junior QC Analyst to join an established pharmaceutical manufacturing team. This is an entry-level position ideal for recent graduates or individuals starting their career in Quality Control. You will support laboratory testing of raw materials, in-process samples, and finished products to ensure they meet required quality and regulatory standards.

• Perform routine analytical testing on raw materials, in-process samples, and finished products following established methods and SOPs.
• Accurately record and report test results in compliance with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).
• Prepare laboratory reagents, standards, and solutions.
• Assist in the maintenance, calibration, and cleaning of laboratory instruments and equipment.
• Support investigations into out-of-specification (OOS) results under supervision.
• Ensure all work is completed within required timelines to support production.
• Maintain a clean, organised, and compliant laboratory environment.
• Follow all health, safety, and environmental procedures.
• Assist with documentation updates and general QC administrative tasks.

• Degree (or equivalent) in Chemistry, Pharmaceutical Science, or a related scientific discipline OR relevant laboratory experience.
• Strong attention to detail and willingness to learn.
• Basic understanding of laboratory techniques.
• Good communication and organisational skills.

• Placement year or internship experience in a laboratory or pharmaceutical environment.
• Basic knowledge of GMP or regulated industries.
• Familiarity with analytical techniques (e.g., HPLC, UV, titration).

If you receive suspicious outreach claiming to be from us, please contact us via the ManpowerGroup website.

Job Title: Quality Control Analyst

Location: Newmarket, England, United Kingdom.

About the Company

We are a leading UK manufacturer of fine chemicals and pharmaceutical intermediates, providing high-quality custom manufacturing and process development services to customers across the pharmaceutical, biotechnology, agrochemical, and specialty chemical industries. As part of our continued growth, we are seeking a motivated and detail-oriented QC Analyst to join our Quality Control team.

About the Role

As a QC Analyst, you will play a critical role in ensuring the quality and compliance of our products. Your key responsibilities will include:

Responsibilities

• Performing routine and non-routine analysis of raw materials, intermediates, and finished products.
• Operating and maintaining analytical instrumentation, including HPLC, GC, UV-Vis, FTIR, Karl Fischer, and wet chemistry techniques.
• Reviewing analytical data to ensure compliance with specifications.
• Preparing analytical reports and laboratory documentation in accordance with GMP and company procedures.
• Investigating Out of Specification (OOS), Out of Trend (OOT), and laboratory deviations as required.
• Supporting analytical method verification, validation, and method transfers.
• Assisting with stability studies and environmental monitoring activities.
• Performing instrument calibration, routine maintenance, and troubleshooting.
• Maintaining laboratory housekeeping and ensuring compliance with Health & Safety procedures.
• Participating in continuous improvement initiatives to enhance laboratory efficiency and quality.
• Collaborating with Production, QA, and Process Development teams.

Qualifications

Essential:

• Degree (or equivalent) in Chemistry, Analytical Chemistry, Pharmaceutical Science, or a related scientific discipline.
• Previous laboratory experience within a pharmaceutical, chemical, CDMO, or GMP-regulated environment.
• Hands-on experience using HPLC and/or GC.
• Good understanding of GMP and laboratory documentation practices.
• Strong attention to detail and excellent organisational skills.
• Ability to work independently and as part of a team.
• Strong written and verbal communication skills.

Desirable:

• Experience working within a pharmaceutical manufacturing environment.
• Knowledge of analytical method validation and transfer.
• Experience investigating OOS/OOT results.
• Familiarity with LIMS, Empower, Chromeleon, or similar chromatography software.
• Understanding of ICH guidelines and data integrity principles (ALCOA+)

Pay range and compensation package

Salary: 28,000 to 36,000 dependent on experience.

Talent STEM are partnering with an established chemical manufacturer to recruit a Temporary QC Analyst to support their Quality Control laboratory during a busy production period.

This is an excellent opportunity for an experienced QC Analyst to join a busy manufacturing laboratory, carrying out routine analytical testing to support production and ensure products consistently meet quality standards.

The Opportunity

Working as part of the Quality Control team, you will perform routine analysis of raw materials, in-process samples and finished products using a range of analytical techniques. This is a hands-on laboratory role within a fast-paced manufacturing environment.

Key Responsibilities

- Perform analytical testing of raw materials, intermediates and finished products.

- Operate GC, HPLC, FTIR and Karl Fischer instrumentation.

- Carry out wet chemistry techniques including titrations.

- Prepare samples, standards and reagents.

- Record, review and report analytical results accurately.

- Support investigations into out-of-specification results.

- Maintain laboratory equipment and documentation.

- Ensure compliance with laboratory quality, HSE and COSHH procedures.

- Work closely with production and technical teams to support manufacturing.

About You

To be considered, you should have:

- A BSc (or equivalent) in Chemistry or a related scientific discipline.

- Previous experience within a QC or analytical laboratory.

- Essential: Hands-on industrial experience operating both GC and HPLC.

- Experience using FTIR and Karl Fischer would be advantageous.

- Wet chemistry experience, including titrations.

- Strong attention to detail and good laboratory documentation skills.

- A good understanding of laboratory safety and quality procedures.

- The ability to work effectively within a busy laboratory environment.

Why Apply?

- Immediate start available.

- Join an established chemical manufacturing business.

- Work with a wide range of analytical techniques.

For a confidential discussion, please contact Talent STEM directly.

Important: Applicants must have the unrestricted right to work in the UK. Unfortunately, this role is not eligible for visa sponsorship, and we are unable to consider applications from candidates who require sponsorship now or at any point in the future.

Talent STEM is a specialist recruitment consultancy supporting the scientific, engineering, chemical, pharmaceutical, environmental, waste, biotechnology, medical device and manufacturing sectors.

Our Client, Located Near to Wellingborough are Seeking an Experienced Senior QC Analyst to join their Pharmaceutical Quality Control Laboratory Team, who are Responsible for Performing Analytical Testing, Conducting Investigations, and Ensuring Regulatory Compliance

ROLE

• Routine and Non-Routine Analysis, Using HPLC and Other Analytical Techniques
• Testing of Raw Materials, Finished Products, Stability Samples, and In-Process Samples
• Accurately Review and Interpret Analytical Results
• Ensure Laboratory Documentation is Completed in Compliance with GMP and Data Integrity Requirements
• Support OOS, OOT, Deviation, and CAPA Investigations
• Participate in Method Validation, Verification, and Transfer Activities
• Maintain Compliance with SOPs, GMP, ICH Guidelines, and CFR Requirements
• Assist with Laboratory Housekeeping, Calibration, and Equipment Maintenance
• Work Collaboratively with Other Site Departments

REQUIRED

• Degree in Chemistry or Pharmaceutical Sciences
• Minimum 5 Years Experience in a Pharmaceutical QC Laboratory
• Hands-on HPLC Experience
• Experience with a Variety of Analytical Techniques eg UV, FTIR, and Karl Fischer
• Sound Knowledge and Experience of GMP, Data Integrity, and Regulatory Compliance
• Experience with Chromeleon or Similar CDS Software
• Strong Analytical and Problem-Solving Skills
• Good Documentation Skills
• Ability to Work Independently and Manage Priorities Effectively
• Experience with Stability Studies and Method Validation
• Exposure to Investigations, Including OOS/OOT

REMUNERATION

• Inckudes Shift Allowance

QC Lab Technician (Weekend Days)

Wigan

Friday to Sunday 6am to 6pm

£35,025

My client, who is a leading manufacturer withing polymers and synthetic resins, is seeking an experienced QC Lab Technician to join their team.

QC Lab Technician

The Role

The main purpose of the QC Laboratory Technician is to ensure the quality of all goods entering or leaving the company.

All aspects of site operations must be completed in a safe, timely and professional manner reporting any problems which arise.

QC Lab Technician

Responsibilities

• Ensure the timely completion of product testing in process and final analysis / specifications.
• Prepare pre-shipment samples and ensure accurate documentation
• Testing of incoming materials, as and when required
• Carry out project / development work when assigned
• Carry out procedures relevant to the test equipment calibration schedule
• Carry out test method training for operators and other assigned deputies
• Issue of accurate process adjustment instructions to production
• Complete inspection and test procedures, as specified in the product manufacturing instructions, and complete the respective quality documents in a timely manner
• Identify non - conforming material or process operations and take action to arrange for re-processing, usage under concession or safe disposal of non - conforming material / product and the completion of the corresponding quality records
• To inform the Senior QC Chemist or QC Lab Manager immediately of any abnormal situation which cannot be dealt with successfully
• To authorise changes in product specifications, formulas, and manufacturing instructions. (In the absence of Works QC Chemist
• Liaise with Senior QC Chemist, QC Lab Manager and/or Managing Director for technical matters and concessions
• Respond to non-conformance corrective and preventive actions (customer complaints, process failures) in a timely manner. Report to Senior QC Chemist or QC Lab Manager regarding such actions
• Immediately report any incident which the management need to address using the appropriate reporting systems in place
• Respond to required corrective and preventive action in a timely manner

• Ensure that all duties/activities associated within quality control department are carried out in compliance to Health, Safety, Environment and Quality management systems

QC Lab Technician

The Candidate

Skills / Knowledge / Experience

Essential

Desirable

Ability to follow chemistry testing techniques

X

Experience working in a busy industrial lab

X

Practical hands-on attitude

X

Strong verbal and written communication skills

X

Willingness to comply with safety and quality regulations, including wearing and maintaining PPE

X

A desire to work with team members to improve processes and product quality

X

Flexible approach to working

X

Excellent attention to detail including housekeeping

X

Calibration

X

Troubleshooting issues with Lab equipment and processes

X

Good understanding of sampling and product testing

X

Experience of working in a chemical / process type industry COMAH site experience would be advantageous

X

Familiar with management systems 9001, 14001 & 45001

X

Ability to complete root cause analysis and contribute to investigation

X

Understanding of chemical processes

X

Qualifications

Essential

Desirable

BTEC / HNC in Chemistry (or equivalent Level 4 qualification in chemistry)

X

Educated to Degree level in relevant subject

X

IOSH Managing Safely

X

First Aid training

X

Internal Auditor

X

QC Lab Technician

Benefits

• 28 days - includes bank holiday entitlement
• Company Pension - Company contributes 3% and the employee contributes 5%
• Healthcare - Eligible for BUPA cover after 6 months probationary period

QC Lab Technician

Key Skills

Quality Coordinator, Quality Lab Controller, Quality Lab Tester, Quality Lab Technician, Quality Laboratory Analyst, QC Laboratory Technician

Please contact Marie Brisson at Winsearch UK for further information - (url removed)

Winsearch acts as an employment agency for permanent staff. We recruit for roles based in Engineering & Manufacturing, Food & Drinks, Pharmaceutical, Supply Chain & Procurement and Professional Services.

View our latest jobs today on our website(url removed) and follow us on LinkedIn.

Manh

INDWIN

Our clients and their customers come from diverse backgrounds and so do we. We hire our people from various walks of life, each of whom make our company stronger with their talent, uniqueness, and expertise. This is what makes our company special; if you want to help us grow and take this ethos to our clients, then we cannot wait to collaborate with you!

The UK has now left the European Union. Any EU, EEA or Swiss citizens living in the UK that wish to remain in the UK post Brexit need to apply to the EU Settlement Scheme. Although the closing date for applications was 30th Jun 2021, if you have not yet applied but believe that you would qualify under the EU Settlement Scheme, the Home Office have confirmed that they will consider late applications. For further information please see (url removed)> Many Thanks

A Quality Control Manager has become available, offering a salary of 40,000 - 45,000 (DOE) plus a competitive benefits package of up to 12% employer pension contribution, life assurance, enhanced sick pay, 33 days annual leave, long service awards and many more!

This global chemical manufacturer specialises in high-quality speciality chemicals, supplying major brands across the fragrance, cosmetics, and personal care industries. They are seeking a Quality Control Manager to join their manufacturing team in Leek.

Salary and benefits available for Quality Control Manager:

• Annual Salary: 40,000 - 45,000
• Up to 12% Employer Pension Contribution
• Days based role
• 33 days Annual Leave
• Life Assurance Policy
• Enhanced Company Sick Pay
• Long Service Awards

Quality Control Manager Role Overview:

You will lead the sites QC function, ensuring laboratory operations, testing activities, and quality systems support safe, compliant, and efficient manufacturing. The role is responsible for developing the QC team, maintaining compliance with customer and regulatory requirements, managing laboratory resources, resolving quality issues, and driving continuous improvement across the site.

Skills and Experience Required from Quality Control Manager:

• Lead and manage the sites QC system and laboratory operations, ensuring effective testing, inspection, and release of raw materials, intermediates, finished products, returns, waste, and environmental samples.
• Oversee QC laboratory resources, equipment maintenance, consumables, and budget planning, including monthly and annual forecasting to meet operational requirements.
• Develop and maintain QC team capability through coaching, training, competency management, and ownership of the QC Competency Matrix.
• Manage product and raw material specifications, inspection data, and concession processes to ensure compliance with quality and regulatory requirements.
• Support supplier approval activities for raw materials and collaborate with suppliers to maintain quality standards.
• Coordinate and support the investigation and timely resolution of customer complaints, driving effective corrective actions and continuous improvement.
• Support the sites ISO 14001 Environmental Management System, including environmental compliance activities and delivery of the internal audit programme

To apply for this Quality Control Manager opportunity, please submit your CV for review. Alternatively, contact Kate Wadsworth at E3 Recruitment for further information.

QC Scientist
Location: Near Peterborough, Cambridgeshire
Job Type: Full-Time, Permanent

Talentmark is recruiting for a QC Scientist to join a growing bioscience organisation operating within a GMP-regulated environment.

This is an excellent opportunity for an analytical scientist with experience in chromatographic techniques to play a key role in quality control testing, supporting the manufacture and processing of high-quality, plant-derived active pharmaceutical ingredients (APIs).

Key Responsibilities:

• Perform analytical testing of plant-derived molecules in accordance with approved SOPs.
• Prepare working solutions, mobile phases, standards, and laboratory reagents.
• Maintain accurate GMP-compliant documentation and ensure data integrity requirements are met.
• Carry out routine maintenance, calibration, and verification of laboratory instrumentation, including GC-MS and HPLC-UV systems.
• Manage laboratory stock levels and consumables to support uninterrupted testing activities.
• Support internal audits and regulatory inspections where required.
• Participate in data review activities and continuous improvement initiatives.
• Collaborate closely with QA, Production, and other cross-functional teams.

• Degree-qualified in Chemistry or a related scientific discipline, or possess equivalent laboratory experience.
• Experience working within a regulated laboratory environment, ideally GMP.
• Familiarity with analytical techniques such as HPLC and/or GC-MS.
• Strong understanding of laboratory safety practices, including COSHH, risk assessments, and PPE requirements.

• Opportunity to join an innovative bioscience organisation with ambitious growth plans.
• Collaborative and fast-paced working environment.
• Work within a modern GMP-regulated laboratory environment.
• Exposure to cutting-edge products and technologies.

QC Chemist required on a permanent basis, based in the Greater Manchester. Requiring proven industrial experience within quality control (QC) testing with wet chemistry techniques, ideally within paints & coatings. A range of other industrial chemical QC experience can be considered.

Title: QC Chemist
Location: Greater Manchester
Salary: 28,000 - 34,000 (dependent on experience)
Term: Permanent

SRG are working with a respected and well-established manufacturer of premium coating products. Renowned for high-quality formulations, expertise and product performance, they are now seeking to hire a QC Chemist to join their technical team in Greater Manchester. This role will be laboratory-based and hands-on, focusing on quality control (QC) testing, batch approval support and technical problem-solving across raw materials, intermediates and finished products. This represents an excellent opportunity for candidates with proven QC or technical laboratory experience within paints, coatings, chemicals or other related manufacturing environments within industrial chemicals.

Benefits: You will join a well-established and highly successful coatings manufacturer. 39 hours per week. 8:30am-5:00pm Mon-Thurs and 8:30am-4:00pm on Friday. 25 days holiday plus bank holidays.

Role / Description

• Perform quality control (QC) assessments on incoming raw materials, products in manufacture and finished goods to ensure compliance with established quality standards.
• Undertake a variety of laboratory evaluations including colour, viscosity, density, pH, gloss, opacity, drying characteristics, adhesion, stability and application performance testing.
• Contribute to batch release activities by interpreting test data, identifying deviations and highlighting any quality concerns requiring further investigation.
• Support the investigation of manufacturing, product quality and customer-related issues, helping to identify root causes and implement effective solutions.
• Assist with colour verification, tint accuracy checks and shade correction activities to maintain consistency across product ranges.
• Produce test panels, drawdowns and application samples to assess both the visual appearance and functional performance of coating products.
• Ensure all laboratory results, quality records, specifications and supporting documentation are completed accurately and maintained in accordance with company procedures.
• Carry out routine calibration, verification and upkeep of laboratory instruments to guarantee reliable and reproducible test results.
• Liaise with colleagues across production, technical and commercial functions to support product quality objectives and continuous improvement projects.
• Provide support with raw material assessments, competitor product reviews and formulation-related activities where required.

Requirements

• Proven industrial experience within a QC, or analytical testing laboratory within the chemicals sector.
  • Experience gained within decorative paints, surface coatings, chemicals or a manufacturing environment would be advantageous.
• A degree, HNC, HND or similar qualification in Chemistry or a related scientific discipline would be beneficial.
• Practical understanding of paint and coatings testing methods including colour, viscosity, pH, density and applied coating performance.
• Excellent attention to detail with strong documentation and record-keeping skills.
• Ability to investigate technical and quality issues and provide practical solutions.
• Good communication skills with the ability to work collaboratively across technical and production teams.
• Knowledge of laboratory safety procedures and quality systems.
• Full UK driving licence would be advantageous.

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 For more information regarding this position or any others, please call Chris on (phone number removed).

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

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

• Job Title: QC Specialist Microbiology
• Location: Speke, Liverpool.
• Hours: M-F, 37.5 hrs p/w
• Rate: 15.04 p/h
• Contract: until end of Dec 2026

SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Microbiologist 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 ideally with some GMP experience to further their career.

Main responsibilities:

• Performing a range of Quality Control tests in line with to GMP regulations.
• Performing routine QC testing: Environmental Monitoring Plates, Utilities Sampling and Testing, Sterility testing Bioburden testing, Selective organism testing Endotoxin testing
• Documenting laboratory results in an accurate and timely manner.
• Complying with GMP regulatory requirements at all times.

Key requirements:

• Educated to BSc /MSc level in a relevant scientific subject
• Industry experience (12 months + desired)
• Experience of working to GMP/pharmaceutical regulatory requirements is highly desirable

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