What Jobs are available for Beverage Production in the United Kingdom?

ECQA is
currently seeking experienced inspectors in England to support our quality control operations for "Diffuser and Candle" products.

Location: Warminster, England, United Kingdom

Type: Freelance / Part-time Inspector

Industry:
Diffuser and Candle

Experience: Prior inspection experience is preferred

Scope of Work:

On-site inspection at warehouse/factory

Check product packaging and labeling

Measure product dimensions

Conduct visual quality checks

Take clear photos

Fill out standard inspection report (template provided)

Requirements:

Based in or near
Warminster, England

Familiar with product quality control procedures

Knowledge of AQL standards

Responsible, detail-oriented, and punctual

Able to follow inspection protocols and meet reporting deadlines

CV submission deadline: September 22, 2025

Interested or know someone suitable?

Please send your CV to

Let's connect and collaborate

Requisition ID: 60790

Position Type: FT Fixed Term

Workplace Arrangement: #LI-Onsite

Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.

This is a fixed-term, onsite position based in Portadown, Northern Ireland, running until the end of August 2026, with the potential for extension.

The site specialises in the production of cheese blocks, sliced cheese, and grated cheese bags.

As a Quality Control Specialist, you will support the technical team by conducting routine inspections, monitoring production processes, and ensuring compliance with food safety standards. You'll assist with audits, equipment calibrations, data reporting, and documentation management. The role also involves cross-functional collaboration to uphold site standards and contribute to quality improvement initiatives.

As a Quality Control Specialist, you will:

• Play a key role in maintaining product integrity and food safety standards
• Conduct routine inspections and monitor production processes
• Support the technical team with problem-solving on the factory floor
• Assist with equipment calibrations and preparation for external audits
• Carry out internal audits including glass & perspex, pest control, and temperature checks
• Trend and report data, including results from the daily Taste Panel
• Manage samples, traceability documentation, and ensure technical records are audit-ready
• Collaborate with all departments to uphold site standards
• Contribute to ongoing quality improvement initiatives across the site
• Perform other day-to-day tasks as requested to support quality and technical operations

• Experience in a food manufacturing or quality control environment
• Solid understanding of food safety standards and regulatory compliance
• Familiarity with laboratory testing methods and equipment
• Competence in using Microsoft Office and quality management systems (e.g., SAP, QMS)

• 25 days annual leave (excluding bank holidays)
• Matched pension scheme
• Access to our employee development platform and Udemy learning resources
• Benefits platform offering discounts and cashback at major retailers
• A collaborative and inclusive work environment with opportunities for career growth

Kerry is an Equal Opportunities Employer. Consistent with our policy of providing equality of opportunity for all, we are required to seek particular information from applicants. As part of your application you will be asked to answer a short number of questions. This information will be held separate to your application and treated in the strictest of confidence.

Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a "starter kit," investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.

Recruiter: #LI-MU1

Posting Type: LI

At OSI Electronics UK, we deliver end-to-end electronic manufacturing services—from design and prototyping to PCB assembly and full box builds. Serving both domestic and international markets, we pride ourselves on producing high-quality, reliable products with outstanding customer support and timely delivery.

Role Summary

We are seeking a proactive and experienced Quality Engineer to strengthen our site’s quality function. This role is key to driving continuous improvement across quality standards and ISO systems.

You will be responsible for developing, implementing, and maintaining robust quality assurance and control systems. This includes defining standards, inspection methods, and procedures to ensure the precision, accuracy, and reliability of our products.

Key Responsibilities

• Lead quality initiatives to support continuous improvement and ISO compliance.
• Define and implement inspection, testing, and evaluation procedures.
• Review engineering designs to incorporate quality requirements.
• Act as the primary contact for shop floor quality issues (mechanical fit, process quality, component specifications).
• Conduct investigations and enforce rapid containment and long-term corrective actions.
• Compile and present regular quality reports to the Quality Manager and relevant teams.
• Analyse production data and develop key quality metrics.
• Support production teams with technical guidance to meet quality standards.
• Communicate quality-related information across internal and external stakeholders.
• Complete First Article Inspection Reports (FAIRs) per customer specifications.
• Liaise with suppliers to ensure incoming goods meet quality standards.
• Manage customer, supplier, and internal quality concerns using 8D corrective action reports.
• Conduct internal and external audits.

Candidate Profile

• HNC qualification or equivalent.
• Minimum 5 years’ experience in electronics manufacturing.
• Solid understanding of ISO9001, ISO14001, ISO13485, and Lean Manufacturing principles.
• Strong IT skills and data analysis capabilities.

QC Engineer

Hinkley Point C, HPC

With a track record of 50 years in the nuclear energy sector, Boccard is ideally placed to serve this new era of nuclear as a leading specialist in engineering, manufacturing, construction and maintenance across the energy industry.

To support our continued growth, Boccard are looking for a qualified QC Engineer to work onsite at HPC. The QC Engineer is responsible for carrying out inspections and surveillance in accordance with the Project Quality Plan. To develop, foster and promote a culture with the client of operational satisfaction. They will support QC Inspectors with daily tasks and create lifetime records, while playing a key role to develop, foster and promote a culture with our client of operational satisfaction.

Key responsibilities

1. Ensure that the Project Quality Plan / Inspection Test Plan is written in-line with the project requirements and is being effectively implemented and shared with relevant managers.
2. Review of all documentation, LTRs & final certification packages are in accordance with contract requirements
3. Review calibration and test equipment are in full compliance with company & contract requirements.
4. Ensure weld procedures comply with relevant code & contract requirements.
5. Carry out any Quality Awareness Training.
6. Analyse non-conformance reports
7. Final review of all fabrication and assembly documentation before submission to the client
8. Maintain the approved suppliers listing and requesting any documentation that may have expired.
9. Liaising with Suppliers, Subcontractors, clients etc and attend meetings where appropriate.
10. Issue of any Quality Documents required by client to Document Control for approval/review.
11. Liaise with sub-contractor and ensure all documentation runs concurrently with the project requirements.
12. Liaise with client representatives relating to QA/ QC operation
13. Conducting Audits of the Works and Projects Quality System, including Sub-contractors and Supplier systems where appropriate. Issuing NCRs where applicable and ensure that they are addressed in a timely manner
14. Review and recording of all Quality Questionnaires and supporting documents for additional Suppliers and Subcontractors wishing to be added to the HPSL ‘Approved Supplier Listing’
15. Colette and keep upto date SQEP Files for HPSL Personnel – issue to client if required by Contract/Client.
16. To carry out any other reasonable duties within the overall function of the role.
17. To be fully aware and comply with Boccard UK Ltd’s policy on Equality & Diversity

Qualifications and Experience

• Advanced knowledge of modern welding procedures
• Excellent communication skills with a good eye for detail
• Significant experience in working on pipe spooling contracts
• Knowledge of RCCM manufacturing specifications
• Computer literate and willing to train on internal digital plat
• forms
• Previous Nuclear experience preferred
• CSWIP 3.1 minimum
• PCN Level 2 MPI – Preferred
• PCN Level 2 UT– Preferred
• PCN Level 2 Radiographic Interpretation– Preferred

Compensation and Remuneration

• A highly competitive salary
• Pension scheme
• 25 days annual leave
• On-going investment in your training and development
• Life Assurance x4 salary
• Employee Assistance Programme

Role: Quality Control Reviewer

Business Unit: Bioscript Regulatory Writing

Location: Macclesfield / London (Hybrid or remote - UK)

About Us

Established in 2005, Bioscript Group is formed from multiple, specialist businesses to support our global pharmaceutical clients; we draw on their multidisciplinary expertise to help navigate critical decisions at key points in the product lifecycle.

Our scientific and strategic expertise helps our clients make better decisions. We provide medical communication services, market access consulting and regulatory writing support with deep domain expertise to effectively navigate complex disease areas.

The Opportunity

The role of the Quality Control Reviewer is to conduct quality control (QC) and other supportive activities to support delivery of accurate, compliant and submission-ready documents prepared by writers in Bioscript Regulatory Writing (including internal and external writers), or by clients.

Key Responsibilities

• Perform QC review and manage QC projects in accordance with agreed upon timelines.
• Verify accuracy of document content using source documents including, but not limited to, clinical regulatory documents (e.g. protocols, clinical study reports, CIOMS reports, clinical summaries/overviews), statistical analysis plans and data tables, figures, and listings.
• Verify internal consistency within a document and across related documents.
• Verify uniformity and compliance of documents with internal or client standards (e.g. document templates, style guide, publishing requirements).
• Record QC findings and identify appropriate corrections to address findings.
• Collaborate with document authors and other team members (as needed) to resolve QC findings.
• Proactively share knowledge and experience to support transfer of knowledge across the team.
• Take responsibility for ensuring optimum use of own time. Flag capacity or bottlenecks to the QC Manager so that resource can be allocated most efficiently. Efficiently manage competing projects, proactively flagging potential issues to the QC Manager.
• Support the Project Management team by monitoring the progress of all assigned projects against the agreed QC schedule and QC budget specification.
• Support the regulatory writing team (eg, supporting other QC Reviewers, editorial support for writers (eg, populating tables, drafting narratives etc).
• Understand QC and publishing processes and strategy, client procedures, and best practice for projects.
• Proofread, edit, compile, and publish regulatory documents according to BRW or client conventions and applicable regulatory and industry guidance.
• Ensure adherence to agreed client/Bioscript standard operating procedures.

About You

• Previous experience working as a QC Reviewer / Regulatory Writer within an agency or pharmaceutical setting
• Previous experience of document publishing preferred
• Attention to detail to ensure accuracy and quality in all deliverables
• Ability to take initiative and manage multiple tasks independently
• Strong communication skills

Our people are at the heart of our business

We are focused not just on delivering the exceptional for our clients, but for our teams too. We understand everyone is different and believe in treating everyone as an individual with opportunities to develop your skills and career around our disciplines.

Our benefits include:

• Salary which aligns with your experience and skillset
• 25 days holiday + bank holidays + winter shutdown + holiday purchase scheme
• Enhanced sick and compassionate leave
• Enhanced maternity, paternity & adoption leave
• Birthday charity donation to a charity of your choice
• Bonus Day off to be spent giving back to the community
• Life Insurance and Critical Illness cover
• Private Medical (Vitality for UK based colleagues)
• Health cash plan or wellbeing allowance
• International Employee Assistance Program

We are committed to creating an inclusive and diverse workplace. We encourage applications from all individuals who meet the minimum requirements of the role. If you require any reasonable adjustments during the application or interview process, please contact us via or by calling .

Blatchford is a multi-award-winning, global, manufacturer of some of the world’s most advanced prosthetic technology, bespoke seating solutions and orthotic devices.

Our evidence-based approach and commitment to continuously challenge possibilities ensures our mobility solutions prioritise the wellbeing and long-term health of our users. Through innovation, science, technology, and maintaining a clear focus on people, we make mobility possible.

We have an exciting opportunity for a Quality Control Engineer to pro-actively pursue continuous quality improvement activities, providing QC engineering/technical support as required.

***This role is initially offered on a 6 month, fixed-term-contract basis***

The role:

As Quality Control Engineer , you will continually improve the qualitive and quantitative activities throughout the Quality Control Department; to aid and assist the Company in its journey to become “Best in Class”.

Key duties and responsibilities :

• Programming, operating and managing CMMs and all related tasks.
• Writing and proving out own programmes without supervision.
• Producing, interpreting and analysing CMM results
• Carrying out investigations as required
• Assisting where required in quality improvement with subcontractors and suppliers
• Maintenance and management of the current company CMM programmes
• Assisting in the pursuit of companywide ownership and implementation of quality improvement and corrective action systems
• Investigating new or alternative Methods of Inspection
• Design tooling and fixturing as required for new and existing products
• Creating CAD models and drawings
• Reverse engineering of CMM fixtures when required
• Liaise with suppliers to manufacture fixtures

What are we looking for?

As Quality Control Engineer , you will have the following:

Key skills and experience:

• Degree or OMC/HNC equivalent
• Working knowledge of ISO9001, ISO13485
• MS Office experience to a minimum of intermediate level
• Programming Starrett Video Measuring Machine (VMM)
• Good working knowledge of SolidWorks software
• Strong communicator with good interpersonal
• Analytical skills
• Ability to work as part of a team and independently with minimum support

What can we off you?

As Quality Control Engineer , you will receive the following:

Benefits

• Competitive salary
• 25 days holiday – increased after service.
• Option to purchase additional annual leave.
• Pension
• On demand pay
• Health cash plan
• Discounted shopping/leisure activity vouchers
• Cycle to work scheme
• Opportunity to be part of an award-winning organisation with a culture that centres around our core values; courage, learning, integrity, collaboration, and innovation

• 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

With more than 150 years of industry-leading experience, the businesses of SGS & Co and SGK are uniting to form SGX—a powerful force in innovative packaging production. Building on the legacy of trusted service since 1947 and 1953, SGX will deliver the full suite of packaging graphics, plate and cylinder production, and metal deco services to brand owners, retailers, and printers—all with a focus on reducing complexity, delivering flawless in-market execution, and leveraging global reach to drive consistency and impact at scale.

We are looking for an Artwork and Repro QC to join the team. The role is responsible for checking a first generation artwork or final print ready file, to ensure it accurately matches the client's design and specification, guaranteeing colour accuracy, high resolution, and technical accuracy before mass production. Pantone matching for consistent brand colours. The QC ensures the final product meets client expectations and technical requirements.

DO

• Ensure that all quality standards have been met on assigned Production components, with limited guidance from the client project team
• Validate that all inputs and instructions have been executed
• Execute digital and analogue techniques to confirm final product meets project standards and complies with technical specifications, copy content and regulatory requirements.
• Ensures the Production team achieves published on-time delivery, ENCP, and/or INCP Production requirements.
• Signed QC checklists may be leveraged to ensure completeness and accuracy of work

DISPLAY

• Focuses on Service - Does things right the first time. Delivers high-quality on time.
• Demonstrates Accountability - Takes ownership for work and outcomes, makes sound decisions, and follows through with commitments. Provides accurate, quality work consistent with standards and expectations.
• Responds with Agility - Stays positive and productive during change. Supports new approaches and helps identify and address barriers to change.
• Creates Value Through Improving Continuously - Looks for ways to drive efficiency, creative thinking, or operational excellence. Technical Capabilities
• Ability to determine correct element position and size, correct font type and size according to master files, style guides/knowledge documents or briefs.
• Basic to proficient experience in photo and color manipulation techniques and processes
• Ability to perform QC check multi-channel artwork (all formats) Inc. spot and technical seps.
• Ability to perform QC check in all standard print production formats (offset, flexo, gravure)
• Able to learn and use QC assistance software such as TVT or Informa IT, etc.

DELIVER

• Establishes high quality standards for all production processes, workflows and client deliverables. Ensures accurate, consistent, and timely completion of high quality, basic to intermediate level artwork, effectively using industry standard software, tools, and prepress and print techniques. Responsible for reading, understanding, and applying customer, legal and regulatory specifications.

The businesses of SGS & Co and SGK have united to form Propelis, a go-to-market ecosystem that enables marketers to move their brands forward with greater speed, clarity, and confidence. Our broad range of integrated solutions include brand creative, packaging, print solutions, branded environments, and content production. Services are delivered through our family of brands: SGX, Marks, Equator, Collide, and 5Flow. With a combined legacy spanning more than 150 years, Propelis commences operations with 10,000 employees in 30+ countr