219 Qc Inspector jobs in the United Kingdom

QC Inspector

Aberdeen, Scotland Hunting Energy Services

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Job Description

Posted: 03/10/ :35

Start Date: Not Available

Salary: DOE

Location: Portlethen (Aberdeen), United Kingdom

Level: Experienced

Deadline: 10/10/ :59

Hours: 36.00

Benefits: Competitive

Job Type: Permanent - Full Time

Job Title: QC Inspector

Reporting to: QA Manager – UK Well Intervention

Nature of the Position: Permanent, Full Time

Location: Portlethen, Aberdeenshire

Role Overview:

The job holder will be responsible and accountable for the control and compliance of products within the QA department in accordance with current manufacturing and Quality Assurance procedures, Engineering drawings and customer requirements; this includes visual and dimensional inspections of machined items, rental fleet items and supplier service items. This would cover first-off inspection, API and licensee standard required inspection and final inspection for all Hunting Energy Services product lines.

Key Responsibilities:

  • Responsible for the visual and dimensional inspection of machined items including:
  • First-off inspection
  • In-process inspection
  • Final inspection
  • NDT inspection
  • Drift testing
  • Calibration of measuring equipment
  • Reviewing all documentation supplied with all items that require a Quality inspection
  • Uploading all hardness, non-destructive testing and drift testing results onto Excel spreadsheet
  • Carrying out lifting equipment visual examination and re-certification
  • Raising of non-conformance reports either internal or Sub-con
  • Controlling non-conforming products
  • Carrying out inspection duties across all areas of the manufacturing and supply chain process
  • Liaising with customer 3rd Party inspectors as required
  • Participating in HSE initiatives where required
  • Good housekeeping
  • Special projects as assigned
  • Covering for incoming inspection in the case of absence, holidays
  • Participating in Internal/External audits. Including resolution of any associated CAR's and PIR's
  • Supporting and direct involvement in the process for the appropriate disposition of all non-conforming products.
  • Co-ordinating with manufacturing and other internal departments to define and resolve product or service quality issues
  • Witness pressure tests to verify that equipment is being tested in accordance with the Quality Plan, Customer Requirements or Work Instruction
  • Creation of all inspection reports as per the Quality Plan, Customer Requirements or Work Instruction

Qualifications/Skills and Experience:

Essential:

  • Knowledge of manufacturing within Oil & Gas industry including relevant product knowledge.
  • Good working knowledge of Microsoft Office Programs (e.g. word)
  • SNT-TC-1A vision test

Desirable:

  • Educated to HNC/HND level in relevant subject area (e.g. engineering)
  • Experience of ISO9001, API Q1
  • Dye penetrant inspection level II
  • Magnetic particle inspection level II
  • Knowledge and experience of a Quality Management System, ERP system, ideally Microsoft AX
  • Full UK Driving Licence
  • In depth knowledge of International Quality Codes and Standards
  • Detailed analysis and reporting techniques including the visualisation and analysis of data
  • Formal Quality Auditing qualification

Personal Qualities

  • Excellent communication (both written and oral), influencing and interpersonal skills
  • High degree of commercial acumen
  • Highly professional conduct
  • Ability to prioritise workload and manage time effectively
  • High level of attention to detail
  • Hardworking, dedicated, enthusiastic and motivated
  • Must be willing to travel and able to spend time away from home
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QC Inspector

Greenford, London WestRock Company

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The opportunity:
Responsible for ensuring that all work meets our customer specifications and is produced in accordance with both BS EN ISO 9001 and the pharmaceutical industry standards (PS9000).
Key Accountabilities:
* As a team member, working to schedules for daily despatch, ensuring that quality levels are maintained and customer delivery dates are achieved
* Undertake all duties in accordance with current Standard Operating Procedures (SOPs), Work Instructions (WI) Quality Policies and Health and Safety Laws. Ensure these procedures are adhered to at all times. The job holder should also ensure that they are aware and understand all such policies and procedures.
* Maintain general discipline and report any breach of conduct to the Quality Manager. Work with the Quality Manager to ensure that cGMP is adhered to and maintained throughout all Departments.
* Set and ensure that a high level of housekeeping to Pharmaceutical Standards is maintained by all staff
* Ensure that Production Batch Records (VWT) are correctly completed prior to final inspection and despatch
* Maintenance of all quality/delivery records, collation and filing / scanning on a daily basis and ensuring that all records are archived on a regular basis
Personal Attributes:
* Numerate and literate (Maths & English at GCSE Grade C or above)
* Previous quality experience (ideally in a carton manufacturing environment)
* Numerate and literate (Maths & English at GCSE Grade C or above)
* Computer literate
* Good communication skills
* Self-motivated
* Ability to work under pressure
* Keen eye for detail
* Team player
* Decision maker
* Knowledge of the print process
* A recognised auditing qualification
* An understanding of ISO9001 standards / PS9000
Health & Safety
* Taking reasonable care for the health and safety of self and others and working with due regard to the responsibilities detailed in the companyu2019s Health & Safety Policy Statement.
* Take the lead with regards to any H&S issue throughout the department, ensuring that all staff are complying with the company procedures
Smurfit Westrock (NYSE:SW) is a global leader in sustainable paper and packaging solutions. We are materials scientists, packaging designers, mechanical engineers and manufacturing experts with a shared purpose: Innovate Boldly. Package Sustainably. Guided by our values of safety, loyalty, integrity, and respect, we use leading science and technology to move fiber-based packaging forward.
Smurfit Westrock is an Equal Opportunity Employer. We strive to create and maintain a diverse workforce where everyone feels valued, respected, and included. Smurfit Westrock does not discriminate on the basis of race, color, religion, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other basis protected by federal, state or local law.
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QA / QC Inspector

Kingston upon Hull, Yorkshire and the Humber BILFINGER

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Job Description

permanent


QA / QC Inspector

Location: Kingston upon Hull

Bilfinger UK is a leading engineering and maintenance provider, supporting customers across the chemical & petrochemical, nuclear, oil & gas, pharmaceuticals & biopharma, power & energy, utilities, renewables and food & beverage markets. We enhance the efficiency of assets, ensuring a high level of availability and reducing maintenance costs.

We have extensive experience in offshore and onshore facilities; specialising in asset management services throughout all life cycle phases from consulting, engineering, manufacturing, assembly, operations, maintenance, and decommissioning.

This commitment is delivered by an experienced and highly competent workforce of over 4,500 employees operating from 14 offices in strategic industrial hubs, upholding the highest standards of safety, compliance and quality.

Mitsubishi Chemicals UK are to build a new production plant adjacent to their existing plant on Saltend Chemicals Park in Hull, named the PUMA project.

The QA / QC Inspector is responsible for ensuring the quality, safety, and integrity of piping systems installed on the PUMA construction project. The inspector will perform regular inspections, assessments, and tests on piping systems to ensure they meet industry standards, regulations, and customer specifications. This position requires attention to detail, strong technical knowledge, and the ability to work independently or as part of a team.

You will be site based in the PUMA project offices.

This position offers the opportunity to contribute to the successful delivery of large-scale construction project, ensuring the quality and safety of all piping systems.

As a QA / QC Inspector, your activities will include the following:
  • Inspect and assess the installation of piping systems in accordance with relevant codes and standards (e.g., ASME, ASTM, API, ANSI)
  • Conduct visual inspections to detect any defects or damage in piping, welds, fittings, and supports
  • Review and interpret piping isometrics and PIDs to ensure proper installation and alignment
  • In-depth knowledge of welding codes and standards (e.g., ASME, AWS, API)
  • Ensure non-destructive testing (NDT) such as ultrasonic testing (UT), radiographic testing (RT), and magnetic particle testing (MPT) of welds are carried out in accordance with the project specifications
  • Conduct visual inspections of welding quality, including surface conditions, alignment, and weld size
  • Verify that all welding is performed according to established procedures and welding standards.
  • Carry out visual inspections and thickness checks on structural and piping coatings
  • Ensure compliance with safety regulations, environmental standards, and quality control procedures during inspections
  • Prepare inspection reports, documenting findings, recommendations, and corrective actions required
  • Collaborate with engineers, project managers, and contractors to address any issues found during inspections
  • Ensure that all necessary documentation is completed accurately and in a timely manner, including inspection records, non-conformance reports
  • Conduct final acceptance inspections for completed piping systems
  • Stay updated on industry standards, codes, and best practices

Qualifications
  • CSWIP Level 3.1 (Minimum)
  • PCN Level2 DPI
  • PCN Level 2 MPI
  • Radiograph Interpretation (Preferable)
  • Coatings Inspection Certs – ICORR Level 1 or NACE Level1 (Preferable

If you wish to speak to a member of the recruitment team, please contact .

Mechanical | Bilfinger UK Limited | Permanent | White-collar workers | Professional | Operations

Bilfinger UK Limited

Operations

Permanent

Professional

Bilfinger Operations

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Quality Control Analyst

Dewsbury, Yorkshire and the Humber Network Scientific Recruitment

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Are you looking for some further experience in Pharmaceutical QC? Do you have prior experience with GC & HPLC in a cGMP environment?


A Global Pharmaceutical Manufacturer are seeking a QC Analyst to join the team at their site in Kirklees. This is a 6 month FTC and would be ideal if you are immediately available and looking to add to your existing experience in Pharmaceutical QC.


Role Overview


  • Full Time , 6 month Fixed term Contract. Day Shifts. £27,000pa.
  • Analysis of Raw Materials and Finished Products to SOPs.
  • Utilise analytical equipment , predominantly HPLC & GC.
  • Interpretation and checking of Analytical Data.
  • Monitoring, Calibration and occasional basic troubleshooting/maintenance of instruments and analytical equipment.
  • Preparation of all relevant documentation in line with applicable standards.


Requirements


  • Prior working experience in a cGMP environment using HPLC and GC is essential.
  • Degree or equivalent in relevant scientific discipline (or equivalent working experience) is essential.
  • Ability to work independently in time pressured environment.
  • Excellent communication skills and attention to detail.


In return


This 6 month FTC is an excellent opportunity to add some additional experience to your CV, working alongside industry leaders in a well renowned pharmaceutical organisation.


For more information, please contact Louis Williams


If this QC Analyst job is not quite right for you, but you’re interested in similar opportunities, please take a look at our other Jobs in the Pharmaceutical Sector. Network Scientific is a multi-award-winning recruitment agency dedicated to connecting top talent with opportunities across the scientific and technical sectors. We specialise in temporary, permanent, and contract placements, and pride ourselves on being an ethical and knowledgeable consultancy with a strong focus on candidate care.

Please note that all applicants for this role should be able to prove that they are legally entitled to work in the country specified. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

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Quality Control Inspector

Deeside, Wales Employment Solutions

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Job Description

A Quality Inspector (Weld & NDT) role is pivotal in upholding quality standards and compliance within manufacturing environments. Responsible for inspections and documentation review, this position fosters a culture of operational satisfaction and adherence to project requirements.


Who this job would suit:

Ideal for CSWIP 3.1 & PCN Level 2 certified QA/QC professionals with meticulous attention to detail and excellent communication skills. Suitable for those experienced in welding procedures and quality assurance protocols, who thrive in collaborative environments.


Key Responsibilities:

  • Complete inspections to ensure material at goods inwards meet the required standards.
  • Liaise with sub-contractors and treatment works to carry out inspections of sites.
  • Visit suppliers and produce relevant inspection reports.
  • Utilise your Welding inspection and NDT knowledge to ensure work is completed to a safe and high standard in compliance with company and ISO standards are followed.

Requirements:

  • CSWIP 3.1 certified is essential.
  • PCN Level 2 in MPI & DPI essential
  • Experience within Nuclear, MOD or Heavy Fabrication is highly advantageous.


Permanent

Pay rate: £24.11 per hour (47k basic) + Overtime at premium rates + Bonus! (OTE circa £55k+)

Location: Deeside

Working Hours: 37.5 hrs (Mon-Thurs), (Fri)


Contact Details:

For inquiries or to apply, please contact Jacob on or

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Analyst, Quality Control

Oxford, South East Moderna

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The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.

As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives.

Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience, with the potential to make a significant impact on patients' lives worldwide.

Moderna's mission is to establish a leading-edge research, development, and manufacturing facility at Harwell, as part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic, NHS and government partners across the UK. We're looking for global experts eager to join us in this endeavour, contributing to a future where access to life-saving vaccines is a reality for all.

This position, reporting to the Associate Director, Quality Control, is an essential part of the Harwell QC team focused on GMP-compliant stability and analytical chemistry testing. As a key contributor, you will support critical release and stability testing operations and play a major role in the management of global stability programs. You will operate and maintain a suite of sophisticated instrumentation, manage cGMP documentation, and support the timely delivery of results across the QC chemistry function. The role offers direct involvement with cutting-edge analytical techniques, stability data management, and regulatory compliance frameworks — as well as exposure to Generative AI tools and digital platforms enhancing Moderna's QC infrastructure.

Here's What You'll Do :

Your key responsibilities will be:

  • Execute routine analytical chemistry and stability testing using HPLC, UPLC, GC, UV, Karl Fischer, particle size analysis (DLS), and other analytical techniques.
  • Support testing across raw materials, components, in-process and drug substance samples.
  • Complete all cGMP documentation for analytical work in full compliance with applicable guidelines.
  • Perform LIMS (LabVantage) data entry and complete electronic assay forms for traceability and review.
  • Carry out HPLC (AEX) and NaOH plate-reader assays in support of manufacturing stat testing.
  • Provide general laboratory support: reagent preparation, inventory management, equipment maintenance, and housekeeping.
  • Ensure safe laboratory operations, actively contributing to EHS compliance.
  • Participate in procurement and stock management of lab consumables and supplies.

Your responsibilities will also include:

  • Conduct stability program operations: set down, pull, labeling, verification, inventory updates, and disposal.
  • Author, review, and revise stability protocols, SOPs, and technical reports.
  • Maintain and trend stability data, performing statistical analyses and ensuring real-time visibility of study progress.
  • Interface with external labs for sample shipment and testing data coordination, and update internal databases and binders accordingly.
  • Support regulatory submissions by contributing to stability sections and ensuring alignment with FDA, EU, and ICH guidelines.
  • Assist with troubleshooting analytical methods and instrumentation as required.
  • Support training and mentorship of junior staff as needed.
  • Contribute to quality systems documentation including investigations, deviations, CAPAs, and change controls.
  • Promote a positive, inclusive, and collaborative culture in line with Moderna's values.
  • Ensure strict adherence to GDP, data integrity, and internal SOPs across all executed tasks.
  • Complete all required training and qualifications in accordance with assigned learning plans.

The key Moderna Mindsets you'll need to succeed in the role:

  • We obsess over learning. We don't have to be the smartest—we have to learn the fastest.

    In this highly technical and regulated environment, your ability to absorb evolving regulatory guidance, apply new analytical tools, and quickly learn from experimental data will be critical to your effectiveness.
  • We digitize everywhere possible using the power of code to maximize our impact on patients.

    With increasing use of Generative AI tools and digital systems like LIMS at the core of Moderna's QC infrastructure, your comfort with digital platforms and data-driven execution will allow you to unlock greater speed, accuracy, and compliance.

Here's What You'll Need :

  • Education: BA/BSc in Chemistry or Biology (preferred) or other relevant scientific discipline
  • Experience: At least 5-7 years in Quality Control Laboratory of a Pharmaceutical Company
  • Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards)
  • This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work.
  • As part of Moderna's commitment to workplace safety, this role may require an enhanced pre-employment check.

At Moderna, we believe that when you feel your best, you can do your best work. That's why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.

  • Quality healthcare and insurance benefits
  • Lifestyle Spending Accounts to create your own pathway to well-being
  • Free premium access to fitness, nutrition, and mindfulness classes
  • Family planning and adoption benefits
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments
  • Location-specific perks and extras

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply

Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at .

LI-DS2
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Quality Control Administrator

Tanpopo

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Job Description

Who Are We?

Tanpopo Japanese Food are a well-established food manufacturing business specialising in Japanese Food based in Feltham who have been operating for over 25 years. We are currently seeking a detail-oriented and dedicated Quality Control and Labelling Assistant (Night Shift, 00:00-08:00) to join our food production team.

As a Quality Control Assistant, you will play a critical role in ensuring that our products meet the highest standards of quality and safety. You will be responsible for conducting inspections, monitoring processes, and maintaining accurate records in accordance with our quality control procedures.

We do not offer sponsorships

Main Responsibilities Will Include:

  • Perform quality control checks in the production area to ensure compliance with company standards and regulatory requirements.
  • Record and monitor probe temperatures during work in progress (WIP) to ensure proper handling and storage of products.
  • Maintain defrosting records, including in-code checks, defrosting methods, and temperature records.
  • Conduct product sanitisation and chlorine concentration checks for high-risk items, along with regular test strip checks.
  • Supervise and manage the cleaning schedules in the production area to uphold cleanliness and hygiene standards.
  • Check products for metal detection by running them through the metal detector.
  • Weigh and verify products as part of daily production specification weight control reports.
  • Maintain records of dressing quantities used during production.
  • Monitor and record fridge and freezer temperatures regularly.
  • Cross-check all production documents and submit weekly reports to the QA department.
  • Report any food safety and hygiene issues to QA Supervisors and Production Managers promptly.
  • Provide monthly updates on internal product rejection rates.
  • Keep track of short-dated and expired raw material stock and inform relevant departments for necessary actions.
  • Perform weekly calibration of internal scales, probes, air temperatures, and dishwasher probes, and document the results – taking corrective actions as required based on calibration results.
  • Handle printing of labels for the entire shift and ensure proper stock count and consumption label updates.
  • Coordinate maintenance for all printers and perform regular cleaning of the printers.
  • Execute label changeovers and update label racks in the production area and the label room.
  • Transfer labels from the label room to the printer room as needed.

What Are We Looking For?

  • Proven experience in a quality control or food production role, preferably in a food manufacturing or processing environment.
  • Knowledge of food safety regulations, quality control standards, and industry best practices.
  • Excellent attention to detail and a strong commitment to maintaining high-quality standards.
  • Proficient in record-keeping and documentation, with strong organisational skills.
  • Effective communication skills to collaborate with cross-functional teams and report any issues promptly.
  • Ability to work independently with minimal supervision and function well as part of a team.
  • Strong problem-solving and decision-making abilities to address quality control challenges effectively.
  • Flexibility to work in shifts and adapt to changing production demands.
  • Ability to work in a fast-paced and physically demanding environment.
  • Basic computer skills, including proficiency in MS Office applications.
  • Food safety certifications (e.g., HACCP, SQF, ServSafe) are a plus.

Benefits:

  • Company pension
  • Discounted or free food
  • Employee discount
  • Free parking
  • On-site parking
  • Referral programme

Pay: £12.50 per hour

Ability to commute/relocate:

  • Feltham TW14 0RB: reliably commute or plan to relocate before starting work (required)

We do not offer sponsorships

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Quality Control Inspector

Inchture, Scotland International Procurement & Logistics Ltd

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About The Role

Join Our Dynamic Onsite Technical Team at IPL Inchture

We are thrilled to announce an exciting opportunity for a Quality Control Inspector to become a vital part of our onsite Technical Team at our Potato site in Inchture. If you are passionate about Quality and are eager to contribute to a dynamic team, this role is perfect for you

Position Details:


• Schedule: Monday - Friday, 7:30am - 4:00pm

• Location: IPL, Inchture - Site Based Role

• Contract Type: Permanent

Key Responsibilities:


• Effectively and efficiently manage the quality of stock from arrival at the site to despatch

• Make decisions on the most effective and efficient use of the product

• Provide the Senior Product Manager with accurate and timely information to communicate to the grower

• Investigate all rejections for their product

• Ensure all reports are completed, scrutinised and progressed on a daily basis

• Interaction with the Packhouse to maintain ASDA Specification and Compliance

• Complete internal audits

What are we looking for?


• Educated to GCSE Level A, B or C (or equivalent) in English and Maths

• Basic knowledge of Microsoft Office programmes such as Word and Excel

• Experience of working in a food manufacturing environment

• Basic knowledge of BRC Auditing

• Basic Food Hygiene Certificate

• Working Knowledge of the PR2 data system

• Assertive (Willing and able to challenge the norm)

• Self-disciplined, Systematic and Precise

What's in it for you?

At IPL, Forza, and Kober , we're dynamic businesses, dedicated to fostering the development of our colleagues and creating an exceptional work environment. We believe in the power of teamwork and collaboration to drive our success. To continue our growth, we're seeking individuals who embody our values, culture, and commitment.

In return, we offer opportunities for professional development, a competitive salary, and a comprehensive benefits package, including:

15% Asda In-store Discount

Paid Annual Leave Allowance – varies depending on shift pattern

Enhanced pension scheme

Life Assurance - All our colleagues benefit from life assurance of 4 x their annual base salary

- Free, direct access to health and wellbeing support service, including unlimited video consultations with a UK-based GP 24/7, physiotherapy, and mental health support

Grocery Aid - We've partnered with Grocery Aid to provide our colleagues and their families with a wide range of emotional, practical, and financial support services

Electric Vehicle Scheme*

Asda Mobile Discount - 30% off a wide range of Asda Mobile bundles and add-ons for our colleagues and one of their family members

Discounted health assessments - We have exclusively negotiated rates on Self-Pay BUPA Health Assessments for you and members of your household

Asda Pet Insurance discount – Up to 10% Discount

Mortgage Advice Bureau (MAB) - MAB can provide fee-free*, no-obligation mortgage and protection advice

Exclusive Exchange Rates via Asda Money - our colleagues can get a better exchange rate for their travel money when buying currency through Asda Travel Money (TravelEx)

Ride-to-work scheme - We work with Evans to provide our colleagues with great savings across their range of bikes, clothing, and equipment

Care Concierge - The Care Experts. Talk to us - we're listening - Legal & General's Care Concierge resource

Plus, lots more Depending on job band, other fantastic benefits are also available including private healthcare, car allowances, and long-term incentive schemes.

Like what you've read? Then do your research, update your CV, and once you're ready, hit the apply button. Don't delay, apply today

About Us

Our purpose here at IPL, Forza & Kober is simple, we are one team who creates exceptional value for our customers and our mission is to support Asda on their journey to becoming #2 in the marketplace.

Through our people we live and breathe our values and we play to our strengths, but we also support each other's development. We are a community of passionate individuals who possess a wide variety of skills and expertise, who work collectively to form a high performing team and a company to be proud of.

We are committed to a fully inclusive business that is representative of our customers, locations and the communities we serve. We recognise the value in diversity and welcome applications from all candidates regardless of sex, age, race, religion, gender or sexual identity and socio-economic background. We are committed to making IPL, Forza and Kober a place where everyone can enjoy a successful career and have systems in place to support all our colleagues. We are seeking applications from candidates who share our values, culture and celebrate diversity in all its forms.

Our culture is our people and our people are our culture

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Quality Control Inspector

ECQA Global Inspection

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Job Description

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

QualityInspection
Diffuser
Candle
QC
Inspection #Hiring
England
Freelance
ConsumerGoods
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Quality Control Specialist

Portadown, Northern Ireland Kerry

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Job Description

Requisition ID: 60790

Position Type: FT Fixed Term

Workplace Arrangement: #LI-Onsite

About Kerry

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.

About the role

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.

Key responsibilities

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
Qualifications and skills
  • 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)
What we offer
  • 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

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