804 Quality Assurance Specialist jobs in the United Kingdom

We require a Quality Assurance Specialist to join our client, based in Hull, on a full-time, permanent basis.  

The Quality Assurance Specialist is an office-based role, which plays a key part in ensuring product consistency across the board, building customer confidence in our client’s offerings, and supporting the delivery of high-quality results that meet client expectations. It also requires a proactive approach in identifying and resolving issues early in the process, helping to maintain operational efficiency and strong client relationships.  

International travel may occasionally be required to carry out supplier audits and support clients’ expectations, resolve complaints, and address product quality concerns.

THE SUCCESSFUL APPLICANT  

• An understanding of marine production quality control practices and standards. Previous experience in quality assessment of pelagic fish is preferred.
li>A minimum of 2 years' experience in a quality processing role.
• Proactive & self-driven.
• The ability to travel occasionally on an ad hoc basis.
• Excellent communication skills.
• Organisation and planning skills, working to deadlines.
• Teamwork, tact, and good interpersonal skills.
• Good geographical knowledge.
• Flexibility and the ability to adapt to changing circumstances.
• Problem-solving ability, particularly when working under pressure.
• Accuracy and attention to detail, able to analyse and monitor outcomes.
• Solid computer skills, including proficiency with Microsoft Office applications.

  JOB DESCRIPTION  

< i>Overall responsibility for delivery of a top-class Quality Assurance programme.
• Create, update and manage quality procedures to ensure standardisation and compliance.
• Coordinate with internal teams to ensure broad quality control coverage and consistent service delivery.
• Analyse inspection reports and raise any quality concerns to ensure prompt action.
• Analyse inspection data to identify trends or areas for improvement.
• Keep detailed records of inspection reports.
• Respond promptly to any incoming quality claims, assess the situation, and on occasions, travel to client sites for effective resolution.
• Be available to handle urgent communications outside regular hours using a company-issued mobile device.

REMUNERATION PACKAGE ON OFFER  

Competitive Salary, bonus opportunities and benefits package.

QEHS Specialist Oakthorpe Dairy

Mon-Fri Days

Looking for an exciting opportunity to make a significant impact in a fast-paced manufacturing company? We are currently seeking an experienced and talented individual to join our Quality, Environmental, Health and Safety (QEHS) team as a key member. As a QEHS Specialist, you will report directly to the QEHS Manager and play a vital role in driving the si.

WHJS1_UKTJ

Are you detail-oriented with a passion for maintaining high standards? Were working with a growing, international manufacturing group to recruit aQuality Assurance Specialistto join their established quality team.

This is a permanent, full-time role offering a structured MondayFriday schedule and a friendly, collaborative working environment. Youll be supporting internal audits, testing routines, a.

WHJS1_UKTJ

Supplier Quality Assurance Specialist

Hertfordshire

£35k - £40k

Drive supplier compliance and quality with these products that millions love. Join as a Supplier Assurance Specialist and make an impact.

There’s a unique kind of rigour in food manufacturing. The pace. The precision. The pressure. And if you’re already working in FMCG, you know exactly what that means. From the first link in the supply chain to the final pack on the shelf, quality isn’t just a box to tick – it’s the foundation.

This is your opportunity to play a critical role in one of the industry’s most performance-driven environments – where operational integrity, supplier compliance, and audit readiness are business-critical. If you understand the technical nuance behind raw material assurance, third-party standards, and supplier risk management, this isn’t just another technical role. It’s a strategic one.

About the Role

As Supplier Assurance Specialist , you’ll be the technical gatekeeper of supplier integrity across a diverse and dynamic FMCG portfolio. You’ll ensure our supplier base – from primary ingredients to indirect materials – not only meets but exceeds internal standards and external regulations. From onboarding and auditing to documentation and performance monitoring, you’ll bring structure to complexity and rigour to compliance.

Reporting into Quality or Technical leadership (depending on the business structure), you’ll be a driving force behind continuous supplier improvement. Think root cause analysis, specification compliance, and collaborative corrective action – not endless box-ticking.

Candidate Profile

You’re already in a supplier assurance, quality, or technical compliance role within food production or FMCG – possibly from a background in raw materials, packaging, or co-manufacturing. You understand BRCGS, HACCP, VACCP, TACCP and supplier risk assessments like the back of your hand.

You’ll likely have a food science, technical or quality qualification, and you’re no stranger to working cross-functionally with procurement, NPD, or regulatory teams. Above all, you combine technical fluency with commercial awareness – balancing compliance with operational pace.

What’s on Offer

Exposure to a fast-paced, commercially ambitious FMCG environment

Influence over a critical area of the supply chain with measurable business impact

A business genuinely invested in ethical sourcing, sustainability, and quality

Ready to Take Ownership?

If you’re driven by purpose, precision, and the challenge of maintaining world-class standards across a complex supplier network, this is your next move. Apply now and take control of the standards that define industry-leading FMCG.

Ref DAC55941

• Developing, implementing, and maintaining the company’s Quality Management System (QMS).
• Ensuring all products and processes comply with current Good Manufacturing Practices (cGMP) and other relevant regulatory standards.
• Conducting internal audits and participating in external regulatory inspections.
• Reviewing and approving batch records, validation protocols, and reports.
• Investigating deviations, out-of-specification (OOS) results, and customer complaints, and implementing corrective and preventive actions (CAPA).
• Managing change control processes and ensuring proper documentation.
• Training personnel on quality assurance procedures and GMP requirements.
• Monitoring key quality metrics and reporting on the performance of the QMS.
• Collaborating with cross-functional teams, including manufacturing, R&D, and regulatory affairs, to resolve quality issues.
• Identifying opportunities for process improvements to enhance product quality and compliance.

• Developing, implementing, and maintaining the Quality Management System (QMS).
• Ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulations.
• Conducting internal audits and supporting external regulatory inspections (e.g., MHRA, FDA).
• Reviewing and approving batch manufacturing records, validation protocols, and reports.
• Managing deviations, CAPAs (Corrective and Preventive Actions), and change controls.
• Participating in product development and lifecycle management activities from a quality perspective.
• Training personnel on quality procedures and GMP requirements.
• Monitoring and analyzing quality data to identify trends and areas for improvement.
• Staying current with pharmaceutical regulations and industry best practices.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 3 years of experience in pharmaceutical quality assurance or quality control.
• In-depth knowledge of GMP, GCP, and other relevant regulatory guidelines.
• Experience with quality management systems, document control, and CAPA processes.
• Strong analytical skills and ability to interpret complex data.
• Excellent written and verbal communication skills.
• Ability to work independently and manage time effectively in a remote setting.
• Proficiency in MS Office Suite and familiarity with electronic quality management systems (eQMS).

• Develop, implement, and maintain the company's Quality Management System (QMS).
• Conduct internal audits and support external regulatory audits (e.g., MHRA, FDA).
• Review and approve batch records, validation protocols, and other quality-related documentation.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
• Manage change control processes to ensure that any changes to processes, equipment, or materials are properly evaluated and documented.
• Oversee supplier qualification and auditing processes.
• Participate in product lifecycle management, ensuring quality standards are met at every stage.
• Provide training to personnel on quality assurance procedures and GMP compliance.
• Stay current with evolving pharmaceutical regulations and industry best practices.
• Contribute to the continuous improvement of quality processes and systems.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A Master's degree is a plus.
• Minimum of 5-7 years of experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, GDP, and relevant regulatory frameworks.
• Proven experience in conducting and participating in audits.
• Strong understanding of pharmaceutical manufacturing processes and quality control techniques.
• Excellent analytical and problem-solving skills with a keen attention to detail.
• Proficiency in using QMS software and electronic document management systems.
• Strong written and verbal communication skills.
• Ability to work effectively both independently and as part of a team in a hybrid environment.
• Familiarity with data integrity principles and practices.

• Review and approve batch records, ensuring all manufacturing and testing activities are documented accurately and comply with established procedures.
• Conduct internal audits and inspections to assess compliance with GMP/GDP and other relevant regulations.
• Investigate deviations, non-conformances, and customer complaints, implementing effective corrective and preventive actions (CAPA).
• Prepare, review, and approve quality-related documents, such as SOPs, validation protocols, and change controls.
• Participate in regulatory inspections (e.g., MHRA, FDA) and assist in preparing responses.
• Monitor quality metrics and identify trends to drive continuous improvement initiatives.
• Provide training and guidance to personnel on quality systems and regulatory compliance.
• Collaborate with cross-functional teams, including manufacturing, R&D, and regulatory affairs, to resolve quality issues.
• Maintain the quality management system (QMS) and ensure its ongoing effectiveness.
• Stay updated on current pharmaceutical regulations and industry best practices.

• BSc or MSc in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 4 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
• Thorough understanding of GMP, GDP, and other relevant pharmaceutical regulatory guidelines.
• Experience with quality management systems, deviation handling, CAPA, and change control.
• Strong analytical and problem-solving skills.
• Excellent attention to detail and accuracy.
• Proficient in using quality documentation software and Microsoft Office Suite.
• Strong written and verbal communication skills.
• Ability to work independently, manage time effectively, and prioritize tasks in a remote setting.
• Experience with auditing or conducting regulatory inspections is highly desirable.