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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.

Site Quality Lead (Quality Assurance)

Salary: 28,000 - 30,000 per annum
Location: Derbyshire
Hours: Full-time Monday to Friday (with a shorter Friday) or the option of a 4-day week (10-hour shifts)

Are you ready to take the next step in your Quality Assurance career?

We're working with a well-established manufacturing business looking to appoint an ambitious Site Quality Lead to oversee quality activities at one of their production sites. Although the title reflects the responsibility of leading quality on-site, this is a hands-on Quality Assurance position, ideal for someone looking to progress into a leadership role.

Reporting to the Group Quality Manager, you'll take ownership of the site's quality systems while supporting and mentoring a Laboratory Technician. This is an excellent opportunity for an experienced QA professional who enjoys being involved in day-to-day quality activities while developing their leadership skills.

Key Responsibilities

• Lead day-to-day quality assurance activities across the site.
• Ensure compliance with quality systems, procedures and industry standards.
• Conduct internal audits, inspections and investigations where required including report writing.
• Manage non-conformances, corrective actions and continuous improvement initiatives.
• Support production teams with quality-related issues and promote a quality-first culture.
• Supervise and support the site's Laboratory Technician.
• Liaise with the Group Quality Manager to maintain consistent quality standards across multiple sites.

About You

• Previous experience within a Quality Assurance role in a manufacturing environment.
• Experience within aseptic manufacturing would be advantageous but is not essential.
• A proactive, motivated individual looking to progress their career.
• Strong attention to detail with excellent problem-solving skills.
• Confident communicator with the ability to influence colleagues across the business.
• Passionate about continuous improvement and maintaining high-quality standards.

What's on Offer?

Salary of 28,000 - 30,000, depending on experience.

33 days annual leave including Bank Holidays (pro rata equivalent for a 4-day week).

Flexible working pattern with the option of a 4-day working week (10-hour days).

Company benefits package.

Genuine opportunity to develop into a broader quality leadership role.

Supportive management team and excellent career progression opportunities.

If you're an enthusiastic QA professional looking for your next challenge and the opportunity to make a real impact within a growing manufacturing business, we'd love to hear from you.

Please note: This opportunity is currently being handled on a confidential basis. Full details of the company will be provided to shortlisted applicants.

Position: Quality & Compliance Manager
Location: Lowestoft, Suffolk (Travel required)
Salary: 55,000 per annum + Welcome Bonus + Monthly Car Allowance + Employee bonus
Hours: Full Time, Permanent

Careermakers are proud to be recruiting for an experienced Quality & Compliance Manager on behalf of a leading provider based in Lowestoft.

This is an exciting opportunity to join a highly respected organisation, supporting care homes across the region to drive quality, compliance and continuous improvement while ensuring exceptional, person-centred care is delivered.

Benefits as a Quality & Compliance Manager:

• Pay increase with longevity
• Welcome bonus
• Generous paid annual leave
• Monthly Car Allowance
• Performance Related Pay (PRP)
• Company pension
• Ongoing training and career development
• Opportunity to work for an award-winning care provider

Responsibilities as a Quality & Compliance Manager:

• Provide coaching, guidance and support to Home Managers across multiple care services.
• Lead on audits, quality reviews, compliance monitoring and improvement plans to drive service excellence.
• Analyse performance data, identify development areas and work with teams to promote safe, compassionate and high-quality care.

Requirements as a Quality & Compliance m:

• Previous experience in a quality, compliance or operational management role within health or social care.
• Strong knowledge of CQC regulations and governance frameworks.
• Experience supporting or managing multiple services.

Are you an experienced quality or operational leader looking to make a real impact across multiple care services?

APPLY NOW to find out more or contact Umay at Careermakers Healthcare today!

Please note: This position does not offer any sponsorship

We are working with an established pharmaceutical company who are looking to employ a Quality Control Analyst, permanently in the Sandwich area.

PLEASE DO NOT APPLY IF YOU DON'T LIVE LOCALLY TO SANDWICH, KENT AND HAVE A FULL RIGHT TO WORK WITH NO RESTRICTIONS (NO GRADUATE VISAS/SPONSORSHIP/RELOCATIONS PLEASE)

This is an exciting full-time permanent position, 37.5 hours per week, 8.30am to 5pm, with an hour's lunch. Competitive salary of 29,000 per annum, plus a host of benefits, to include:

• 31 days annual leave, inclusive of Bank Holidays.
• Auto enrolled pension scheme
• Healthcare, Death in Service, Private Medical insurance including dependants
• Annual bonus scheme
• Free parking
• Great working environment

You must be committed and have HPLC experience. Support the production and QA Departments in ensuring all aspects of the manufacture of products are performed in a controlled manner, meeting commitments to international regulatory bodies, as well as Good Manufacturing Practice. Ensure manufactured products are compliant and fit for purpose by performing physical and analytical testing and report accurate results. Duties to include:

• Being responsible for physical analytical testing.
• Follow internal methodologies.
• Adherence to GMP requirements.
• Accurately record microbiological results within data packages, as received.
• Execution of protocols.
• Ensure laboratory housekeeping standards are maintained and documented accurately.
• Ensure all equipment is suitable for use.

Requirements:

• A relevant BSc degree, e.g. Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics, or equivalent.
• Experienced in QC testing of API, including HPLC and GC.
• 2+ years' experience in a similar position.
• Previous GMP laboratory experience.
• Good attention to detail, able to prioritise workload, positive and flexible approach.

Local candidates need only apply and those with no restrictions on their right to work.

New Appointments Group, Expertly Matching Employers and Jobseekers since 1975.

If this role isn't for you, please check out our website for other opportunities that may be suitable, or send us your CV, we'd still like to hear from you. You can find us on our website or on LinkedIn, Facebook, Instagram and

We are committed to fostering a diverse and inclusive environment in line with the Equality Act 2010. All qualified applicants will be considered regardless of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, religion or belief, sex, or sexual orientation. New Appointments Group acts as an Employment Agency for permanent roles and as an Employment Business for temporary roles.

Change Control & Quality Specialist

Location: Folkestone
Job Type: Full-Time Temporary

Are you an experienced Quality professional with a passion for driving change, maintaining compliance, and improving quality systems? We're recruiting on behalf of a leading international manufacturer for a Change Control & Quality Specialist to join their European Quality team on a 6 month Temporary basis.

This is an exciting opportunity to play a key role in managing change control activities across Europe while supporting continuous improvement initiatives within a highly regulated environment.

The Role

Reporting to the European Head of Quality, you will be responsible for overseeing the European Change Control programme, ensuring quality processes remain compliant with GMP and regulatory requirements. You'll work collaboratively with teams across Europe and globally to deliver successful change initiatives and maintain an audit-ready quality management system.

Key Responsibilities

• Lead and manage the European Change Control programme for temporary and permanent changes.
• Review change requests, assess business impact, and ensure compliance with GMP and applicable regulations.
• Coordinate stakeholders throughout the change control process.
• Monitor progress of change actions and ensure completion within agreed deadlines.
• Produce KPI reports and analyse change control performance.
• Identify opportunities to improve quality systems and change management processes.
• Deliver training, coaching and guidance on Change Control procedures.
• Maintain audit readiness and support internal and external audits.
• Support quality investigations, CAPA activities and continuous improvement initiatives.
• Assist in the development and maintenance of the Quality Management System (QMS).
• Ensure documentation, records and quality files are accurately maintained.

About You

We're looking for someone who has:

• A degree in Science, Engineering or a related discipline.
• At least three years' experience within a Quality or Technical function.
• Experience working within a regulated industry such as Pharmaceuticals, Medical Devices or FMCG.
• Strong knowledge of GMP and Quality Management Systems.
• Experience managing change control processes and implementing quality improvements.
• Knowledge of ISO 13485, ISO 22716, MDD and MDR.
• Experience supporting audits and regulatory inspections.
• Excellent communication and stakeholder management skills.
• Strong analytical skills with experience producing KPIs and trend analysis.
• A proactive approach with excellent attention to detail and a continuous improvement mindset.

You will be working 37 hours week Monday to Friday based between 2 sites and there may be the opportunity to work 1 day at home once full training is complete

If you're an experienced Quality professional looking to take the next step in your career and make a real impact within a global organisation, we'd love to hear from you.

New Appointments Group, Expertly Matching Employers and Jobseekers since 1975.

Before submitting your CV, please take a moment to check the layout, spelling, and grammar. If your CV includes graphics or design features, we'd also appreciate a simplified version in Word format.

If this role isn't for you, please check out our website for other roles that may be suitable, or send us your CV, we would still like to hear from you! You can find us on (url removed) or LinkedIn, Facebook, Instagram and

We are committed to fostering a diverse and inclusive environment in line with the Equality Act 2010. All qualified applicants will be considered regardless of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, religion or belief, sex, or sexual orientation. New Appointments Group acts as an Employment Agency for permanent roles and as an Employment Business for temporary roles.

Next Step Recruitment Solutions is working with a well-established supported living provider in London to recruit a Quality Compliance Officer. This is a great opportunity for someone with a background in health and social care quality assurance who wants to make a genuine difference to the lives of adults with learning disabilities, autism, mental health needs and other complex support requirements.

You'll work closely with the Head of Quality and service managers, carrying out audits, driving up compliance standards, and helping teams turn audit findings into real improvement.

What you'll be doing:

• Supporting the development and delivery of the organisation's quality improvement strategy
• Monitoring compliance with CQC standards, internal policies and local authority contracts
• Conducting service audits across the organisation
• Working with service teams to build and implement improvement action plans
• Contributing to best practice guidance, policies and procedures
• Supporting staff training linked to quality and compliance
• Maintaining accurate records and reports for the Quality Assurance and senior management team
• Helping prepare for CQC inspections, local authority reviews and internal quality reviews
• Promoting a culture of learning and continuous improvement across all services

What we're looking for:

• Experience in a quality compliance role within health and social care (essential)
• A solid understanding of CQC regulations and supported living frameworks
• Strong organisational and administrative skills with real attention to detail
• Excellent communication skills, able to build relationships at every level
• A genuine commitment to person-centred care

Nice to have:

• NVQ Level 3 (or above) in Health & Social Care
• Experience supporting services rated "Requires Improvement" to improve their audit scores
• Knowledge of support planning, safeguarding, medication management and risk assessment
• Experience in supported living environments

What's on offer:

• Opportunities for professional growth and development
• A supportive, inclusive team culture
• Access to learning and development resources

If you're passionate about quality and compliance in social care and want a role where your work directly improves people's lives, apply today or get in touch to find out more.

QA Microbiologist Irvine, Ayrshire 27,000 - 29,000 + Benefits

Escape Recruitment is working with a well-established manufacturing business in Ayrshire that is investing heavily in its laboratory and quality capabilities. As part of this growth, they are looking to appoint a QA Microbiologist to support the introduction of in-house microbiological testing.

This is an excellent opportunity for someone with commercial microbiology laboratory experience who enjoys a varied, hands-on role within a manufacturing environment. Graduates with a relevant industrial placement are also encouraged to apply.

Reporting into the Quality team, you'll be responsible for carrying out microbiological testing across raw materials, environmental samples and finished products, helping to ensure products meet the highest quality and regulatory standards.

Duties will include:

• Microbiological testing of raw materials, environmental and finished product samples
• Identifying bacteria, yeast and mould contamination
• Environmental monitoring and hygiene testing
• Preparing media and laboratory reagents
• Recording, analysing and reporting test results
• Investigating out of specification results
• Supporting laboratory validation activities
• Maintaining laboratory equipment and consumable stocks
• Working closely with the wider Quality and Laboratory teams
• Supporting continuous improvement within the laboratory

We're interested in candidates who have:

• A degree in Microbiology, Biological Sciences or a related discipline
• Commercial laboratory experience within a manufacturing environment
• Experience of microbiological testing techniques
• Good laboratory documentation and reporting skills
• Strong attention to detail and organisational skills
• The ability to work both independently and as part of a team
• The right to work in the UK without sponsorship

Graduates who have completed a substantial industrial placement within a commercial laboratory are also encouraged to apply.

• Salary of 27,000 - 29,000
• Opportunity to join a growing manufacturing business
• Modern laboratory environment
• Excellent opportunity to develop within Quality and Microbiology
• Full-time permanent position based in Irvine

If you're looking for your next opportunity within microbiology and quality, we'd love to hear from you.

Walker Cole International is supporting a growing pharmaceutical organisation in the search for a Quality Assurance Officer to join their Quality team on a 12-month fixed-term contract. This is an excellent opportunity to join a rapidly expanding business that has experienced significant growth in recent years, offering exposure to a diverse portfolio of pharmaceutical products and medical devices supplied across European markets.

Operating within a virtual pharmaceutical model, the company works closely with Contract Manufacturing Organisations (CMOs), providing broad exposure to external manufacturing and quality assurance activities. This role offers a hybrid working pattern and the opportunity to develop within a collaborative and supportive Quality team.

You will be responsible for:

• Reviewing batch manufacturing and packaging records to ensure compliance with GMP requirements prior to product release.

• Performing batch release activities, ensuring products meet the required quality standards before distribution.

• Working closely with external manufacturing partners and internal stakeholders to support day-to-day quality assurance activities.

• Maintaining accurate quality documentation while supporting compliance with GMP and the Quality Management System.

The successful candidate will have:

• Previous Quality Assurance experience within a GMP-regulated pharmaceutical, biotechnology or medical device environment.

• Experience reviewing batch records and/or supporting batch release activities.

• A strong understanding of GMP principles and pharmaceutical quality systems.

• Excellent attention to detail, communication skills and the ability to work effectively with both internal teams and external manufacturing partners.

Quality Assurance QA Quality Assurance Officer GMP Good Manufacturing Practice Batch Record Review Batch Release QMS Quality Management System Pharmaceutical Medical Devices CMO Contract Manufacturing Organisation Compliance GDP Hybrid

New Start. is a leading provider of high-quality training and qualifications in Health and Social Care. We are committed to supporting learners and employers to achieve excellence in care through robust training, assessment, and quality assurance.

The Role
We are seeking an experienced?Internal Quality Assurer (IQA)?to oversee the delivery and quality assurance of Health and Social Care qualifications, including the?Level 5 Diploma in Leadership and Management for Adult Care and Residential Childcare. This is a pivotal role ensuring our programmes meet regulatory and awarding organisation requirements, whilst maintaining the highest standards of practice.

Key Responsibilities

• Lead and co-ordinate IQA activities across our assessor team.

• Maintain compliance with awarding body standards.

• Carry out effective sampling, observations and quality assurance activities.

• Support, mentor, and standardise assessment practices to maintain excellence.

• Lead standardisation meetings and manage continuous improvement strategies (QIP/SAR).

• Prepare for and manage external quality assurance (EQA) visits.

• Contribute to the development of learning and assessment resources.

• Carry out Assessor 1-1s and manage learner allocations.

• Maintain and update all relevant quality assurance documentation and records.

• Identify and address any risks to quality or compliance.

Requirements

• Assessor qualification (CAVA / A1 or equivalent).

• IQA qualification (Level 4 Award in the Internal Quality Assurance of Assessment Processes and Practice).

• Hold a Level 5 Diploma in Leadership and Management for Adult Care (or equivalent)

• Substantial experience of quality assurance within Health & Social Care qualifications.

• Strong understanding of the Level 2 Adult Social Care Certificate, to Level 5 Diploma in Leadership and Management for Adult Care.

• Up-to-date knowledge of relevant legislation, frameworks, and best practice in adult social care.

• Excellent organisational, leadership, and communication skills.

What We Offer

• Competitive pay (up to £25 per hour), 8 hours per week (freelance or employed, negotiable).

• Flexible, remote working.

• Opportunity to influence and shape a high-quality provision.

• Supportive and professional team culture.

Job Type: Part-time

Pay: £20.00 - £25.00 per hour

Expected hours: 8 per week