136 Quality Control Analyst jobs in the United Kingdom

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Quality Control Analyst - Tannochside

Join our Team at Macphie

Let us introduce ourselves - Macphie, an internationally acclaimed family ingredient manufacturer, proudly situated in the picturesque and tranquil landscapes of Glenbervie in Aberdeenshire with sites in Glasgow, Tannochside, and Midlands too. Our expertise spans across a spectrum of delectable delights, including sauces, bakery creations, and heavenly ice cream toppings. We also cater to the evolving culinary landscape with our plant-based and gluten-free offerings. Trusted partners to some of the globe's leading food brands, we are dedicated to transforming ideas and creativity into tangible, delectable solutions.

About the role

Reporting into the QA manager the QA analyst is responsible for ensuring that all products are manufactured to the established quality standard, customer specifications and as per IFS.

Ensuring all records and computer transactions are completed accurately, promptly and efficiently to ensure data is maintained for due diligence and audit purposes.

Collaborating with the on-shift production teams the quality analyst will ensure that product integrity, operational efficiency and factory GMP standards are achieved and contribute to the required food safety standards of Macphie and their customers.

Key accountabilities and responsibilities

• Provide shift cover in the QA laboratory and production facilities (alternating early and late shifts on a rotational basis or as agreed) and, as required. Provide shift cover in laboratory areas during holidays and as agreed.
• Reviewing incoming raw materials meet their specification and confirming that the COA is compliant before releasing the raw materials for use.
• Release of finished goods that are within specification by confirming and assessing online quality standards, set quality and lab assessments as appropriate by product family. Where standards are not achieved or do not meet specification these products will be placed on hold and escalated to the QA and/or technical manager.
• Prevent the use of any faulty measuring equipment that is out-with specification when calibrated.
• Ensure weight/volume control is within legal requirements.
• Ensure that all necessary computer transactions/administration are completed efficiently, maintaining complete and accurate up to date records.
• Assist with the sampling, logging and sending of raw materials/products, water samples and hygiene swabs for external analysis.
• Assess the suitability of returned goods, goods damaged on site authorise their disposition, following prior consultation with the QA manager as necessary.
• To ensure that all measuring, recording equipment used are within effective calibration dates, assisting with internal and external calibration of test and measuring equipment as required. Ensuring measuring and recording equipment is working within the set legal requirements.
• To ensure hygiene and GMP standards are maintained in all production areas and that the TS Facility is inspected and any hygiene concerns are escalated to the production team leader or shift manager before production commences and throughout the shift.
• Assist in the investigations of non-conforming product, customer complaints and audit non-conformances to ensure root cause is identified and actions prevent any recurrence.
• Complete any other reasonable duties as assigned by the QA manager treating this work as a priority over work from other areas.
• Work safely at all times in accordance with company Health & Safety policies, procedures, practices and legislation.

Requirements

Experience & Qualifications:

• Quality assurance/control experience preferable but not essential
• Experience in production and/or manufacturing processes and techniques
• Computer skills: Word, Excel, Outlook, Web based applications, etc

Skills:

• Be a team player
• Have good communication skills  
• Have integrity, initiative and focus
• Be self-motivated  
• Flexible with changing work patterns

Knowledge:

• Basic food hygiene
• Basic understanding and knowledge of health and safety standards and compliance

Benefits

Indulge in the Sweet Perks of Joining Macphie!

At Macphie, we believe in crafting not only delightful culinary experiences but also providing our team with a recipe for success in their professional lives. Here is a taste of how we'll look after you as part of our Sweet Success:

• Annual Leave: Recharge your batteries with a generous annual leave entitlement of 23 days, plus 9 public holidays, giving you a refreshing total of 32 days to explore, relax, and savour life outside of work.
• Profit-Related Pay (PRP): Your dedication will not go unnoticed! Enjoy conditional PRP, aligning with our company's performance and rewarding your commitment to our shared success.
• Pension Perks: Secure your financial future with our pension enrolment, where you contribute 5%, and we match it with a 3% employer contribution.
• Health and Wellness Buffet: We care about your well-being. Access our Employee Assistance Program, a 24/7 GP line, and indulge in our cycle-to-work scheme. Keep your mind and body in top shape with our Leisure Subsidy Scheme and free fruit offerings.
• Eco-Friendly Commute: Embrace sustainable living with our electric car charging stations. Enjoy the convenience of free parking while contributing to a greener planet.
• Lifelong Learning: Cultivate your mind with our company further education scheme and unlock opportunities for personal and professional growth.
• Family First: We support your journey into parenthood with enhanced maternity, paternity, and adoption pay.
• Exclusive Employee Benefits: Revel in exclusive benefits like an education bursary via our employee trust and Funeral Concierge provided by Everest Funeral Concierge Service, a brand-new benefit.
• Beyond Probation: Once you have passed probation over the initial three months, you will then be able to unlock an array of group benefits, including access to our Health cash plan & Westfield Health, permanent health insurance, and 3 x death in service life assurance.

To see all of the Macphie employee benefits please click here .

And now, let us talk about what we need from you:

Like every employer, legally, we require to check and confirm that you have the right to work in the UK. If we offer you a job and you accept, there are some checks that we need to complete before you can start with us. In addition to the above, we will also collect satisfactory employment references.

Closing date for applications: Friday 15th August 2025

Job Title: Quality Control (QC) Analyst

Location: Lancashire
Contract Type: 6-Month Temporary Role
Shifts: Includes day and possibly night shifts

• 20-24 per hour

Smart4Chemicals is recruiting a Quality Control Analyst for a leading polymer manufacturer, to join their team on a temporary 6-month basis. Based at their site in Lancashire, this is a great opportunity for someone looking to gain hands-on experience in a high-performing, well-equipped laboratory environment.

The role involves supporting the QC team with polymer testing and general laboratory analysis, helping to ensure products meet required quality and safety standards.

Key Responsibilities:

• Conduct routine and non-routine testing of materials
• Work in accordance with laboratory safety and best practices
• Accurately record and interpret test results
• Support investigations and troubleshooting of quality issues
• Collaborate closely with production and technical teams

What We're Looking For:

• A degree in a scientific discipline (e.g., Chemistry, Materials Science, etc.)
• Previous experience in a quality control or lab-based role is desirable - particularly in polymer or materials testing
• Strong understanding of laboratory safety procedures and good laboratory practice
• A hands-on, team-oriented attitude with a willingness to take on overtime as needed
• Someone who is flexible and adaptable, with a proactive and reliable work ethic

Job Title: Quality Control (QC) Analyst

Location: Lancashire
Contract Type: 6-Month Temporary Role
Shifts: Includes day and possibly night shifts

• 20-24 per hour

Smart4Chemicals is recruiting a Quality Control Analyst for a leading polymer manufacturer, to join their team on a temporary 6-month basis. Based at their site in Lancashire, this is a great opportunity for someone looking to gain hands-on experience in a high-performing, well-equipped laboratory environment.

The role involves supporting the QC team with polymer testing and general laboratory analysis, helping to ensure products meet required quality and safety standards.

Key Responsibilities:

• Conduct routine and non-routine testing of materials
• Work in accordance with laboratory safety and best practices
• Accurately record and interpret test results
• Support investigations and troubleshooting of quality issues
• Collaborate closely with production and technical teams

What We're Looking For:

• A degree in a scientific discipline (e.g., Chemistry, Materials Science, etc.)
• Previous experience in a quality control or lab-based role is desirable - particularly in polymer or materials testing
• Strong understanding of laboratory safety procedures and good laboratory practice
• A hands-on, team-oriented attitude with a willingness to take on overtime as needed
• Someone who is flexible and adaptable, with a proactive and reliable work ethic

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 
li>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 6 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.

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.

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 
li>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 6 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.

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.

Our client is expanding their innovative anode material manufacturing through strategic partnerships and seeks a Regulatory Compliance Manager . This role will embed critical health & safety, product certification, and quality management systems knowledge into the business to ensure compliance and continuous improvement.
 
The Regulatory Compliance Manager will:

• Lead health & safety compliance in a chemical manufacturing environment
li>Monitor and ensure adherence to current battery standards (UN, IEC, CE) and upcoming regulations (e.g. Battery Passport)
• Develop, maintain, and improve ISO 9001 quality management systems across manufacturing stages
• Liaise with certification bodies, regulators, and auditors, preparing necessary documentation
• Train staff on safety, compliance, and quality protocols
• Review and update compliance policies and SOPs regularly

 
The Regulatory Compliance Manager will have:

li>Degree or HNC/HND in Chemistry, Chemical Engineering, or related discipline
• 3+ years' proven experience in regulatory, H&S, or QMS roles within chemical or battery manufacturing
• Strong knowledge of ISO 9001 and audit readiness
• Experience with battery product standards and regulatory frameworks
• NEBOSH or equivalent health & safety certification preferred
• Excellent communication and stakeholder management skills

 
This is an exciting opportunity to lead regulatory and compliance excellence within a cutting-edge manufacturing environment. If you have a strong background in health & safety and quality systems and want to make a real impact, we'd love to hear from you.
 
Apply now to join a team driving innovation in sustainable battery manufacturing.

WSR are recruiting for a Regulatory Compliance Officer for our reputable client based in London.

Job Title: Regulatory Compliance Officer
Role Type: Permanent Part Time – Around 18 hours per week.
Salary: £43k – £5k pro rata for part time hours + ,(Apply online only) location allowance + excellent benefits
Location: Central London base with flexible hybrid working

Are you someone who thrives on solving complex problems, guiding others through tricky regulations, and making sure sensitive data is handled the right way? If that sounds like you, this role could be the perfect next step in your career.

We're looking for a Regulatory Compliance Officer  to join a team that deals with some of the most interesting – and sometimes challenging – data protection and information rights issues out there. You’ll play a key role in helping colleagues and stakeholders navigate legislation like FOI, GDPR , and the Data Protection Act , all in an environment where security and precision really matter.

Regulatory Compliance Officer  Role Overview:

You’ll be the go-to expert for all things compliance and information rights. That means offering practical advice on things like how to respond to FOI requests, handle ICO complaints, or interpret new guidance or case law. No two days will be the same, and every situation will need a careful, thoughtful approach – but that’s what makes this work so rewarding.

You’ll use your knowledge and judgment to make sure colleagues get clear, accurate advice tailored to the situation at hand. And because this is a space that changes quickly, you’ll help keep the wider team up to speed on legal updates and emerging issues.

Regulatory Compliance Officer Experience, Qualifications and Attributes:

• Strong experience with information rights legislation – and ideally, a practitioner-level certificate in data protection or information governance.
• People skills - You’ll need to explain complex rules in a way that makes sense, and know how to build trust with stakeholders from all kinds of backgrounds
• An interest in central government or public sector work would be beneficial but most of all, we’re after someone who’s confident, adaptable, and cares about getting things right.

Regulatory Compliance Officer  Benefits:

• You’ll be part of a supportive, down-to-earth team that shares knowledge, celebrates wins, and helps each other grow.
• London location allowance
• Civil Service Pension
• Generous annual leave
• Access to training and development
• Hybrid working options for better work/life balance
• You'll be part of a workplace that genuinely values diversity, inclusion , and wellbeing – because when you’re supported, you can do your best work!

 
A quick note on security

Because of the nature of the work, everyone in this role needs to go through Developed Vetting (DV) . If you don’t already hold that level of clearance, our client will guide you through the process once your application is successful.

Please click ‘APPLY NOW’, or call the WSR Team at for more info. We appreciate the time and effort invested in your application.

While we strive to respond to all applicants promptly, we kindly ask for your understanding in case of delays. If you do not hear from us within 10 days of submitting your application, please assume that, unfortunately, you have not been successful this time.

We will however keep your CV on file and review your suitability against any other vacancies we may have available.

Our client is expanding their innovative anode material manufacturing through strategic partnerships and seeks a Regulatory Compliance Manager . This role will embed critical health & safety, product certification, and quality management systems knowledge into the business to ensure compliance and continuous improvement.
 
The Regulatory Compliance Manager will:

• Lead health & safety compliance in a chemical manufacturing environment
li>Monitor and ensure adherence to current battery standards (UN, IEC, CE) and upcoming regulations (e.g. Battery Passport)
• Develop, maintain, and improve ISO 9001 quality management systems across manufacturing stages
• Liaise with certification bodies, regulators, and auditors, preparing necessary documentation
• Train staff on safety, compliance, and quality protocols
• Review and update compliance policies and SOPs regularly

 
The Regulatory Compliance Manager will have:

li>Degree or HNC/HND in Chemistry, Chemical Engineering, or related discipline
• 3+ years' proven experience in regulatory, H&S, or QMS roles within chemical or battery manufacturing
• Strong knowledge of ISO 9001 and audit readiness
• Experience with battery product standards and regulatory frameworks
• NEBOSH or equivalent health & safety certification preferred
• Excellent communication and stakeholder management skills

 
This is an exciting opportunity to lead regulatory and compliance excellence within a cutting-edge manufacturing environment. If you have a strong background in health & safety and quality systems and want to make a real impact, we'd love to hear from you.
 
Apply now to join a team driving innovation in sustainable battery manufacturing.