1,464 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.
• 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  

• 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.

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.
• 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  

• 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.

• Develop, implement, and maintain the Quality Management System (QMS).
• Conduct internal and external (supplier) audits to ensure compliance.
• Manage the change control process and associated documentation.
• Investigate deviations, out-of-specification results, and customer complaints.
• Oversee and track the implementation of Corrective and Preventive Actions (CAPA).
• Review and approve batch manufacturing records and product release.
• Qualify and monitor external suppliers and contract manufacturers.
• Ensure compliance with relevant regulations (GMP, ISO, FDA, EMA).
• Assist in the preparation for and participation in regulatory inspections.
• Promote and foster a strong quality culture within the organization.

• Bachelor's degree in Pharmacy, Chemistry, Life Sciences, or a related field.
• Significant experience (e.g., 4+ years) in Pharmaceutical Quality Assurance or Quality Control.
• In-depth knowledge of GMP, regulatory guidelines (FDA, EMA), and quality management systems.
• Experience in conducting audits and managing change control processes.
• Strong understanding of pharmaceutical manufacturing processes and documentation.
• Excellent analytical, problem-solving, and critical thinking skills.
• Proficiency in investigation techniques and CAPA management.
• Strong written and verbal communication skills.
• Ability to work effectively in a cross-functional team environment.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with GMP (Good Manufacturing Practice) and relevant regulatory guidelines (e.g., MHRA, FDA, EMA).
• Conduct internal audits and participate in external regulatory inspections to ensure compliance.
• Review and approve batch records, validation protocols, and other critical quality documentation.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing CAPAs (Corrective and Preventive Actions).
• Manage change control processes, assessing the impact of proposed changes on product quality and regulatory compliance.
• Prepare and maintain product quality review (PQR) reports.
• Collaborate with cross-functional teams, including manufacturing, R&D, and regulatory affairs, to resolve quality issues.
• Provide training on quality standards and GMP requirements to relevant personnel.
• Monitor quality metrics and KPIs, reporting on trends and areas for improvement.
• Ensure the qualification and calibration of equipment used in manufacturing and testing.
• Stay current with evolving pharmaceutical regulations and industry best practices.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 5 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
• Strong knowledge of GMP regulations and guidelines.
• Experience with auditing, deviation management, CAPA, and change control processes.
• Excellent analytical, problem-solving, and critical thinking skills.
• Proficiency in reviewing technical documents and data.
• Strong written and verbal communication skills, with the ability to effectively interact with various stakeholders.
• Experience with quality management software is advantageous.
• Ability to work independently and collaboratively in a team environment.
• Attention to detail and commitment to maintaining high-quality standards.
• Must be legally eligible to work in the UK.

• Review and approve batch records, validation reports, and other critical quality documentation.
• Participate in internal and external audits, ensuring compliance with GMP and other relevant regulations.
• Investigate deviations, non-conformances, and out-of-specification (OOS) results, implementing corrective and preventive actions (CAPAs).
• Contribute to the development and maintenance of Standard Operating Procedures (SOPs) and quality policies.
• Perform process validation and qualification activities, ensuring products are manufactured consistently and reliably.
• Monitor and assess quality trends, identifying areas for improvement.
• Support regulatory inspections by health authorities (e.g., MHRA, FDA).
• Collaborate with cross-functional teams, including Manufacturing, R&D, and Supply Chain, to ensure quality standards are met.
• Provide training to personnel on quality systems and GMP compliance.
• Manage change control processes, evaluating the impact of proposed changes on product quality.
• Conduct risk assessments related to manufacturing processes and product quality.
• Maintain a comprehensive understanding of relevant pharmaceutical regulations and guidelines.
• Prepare quality metrics reports for management review.
• Ensure all activities are conducted in accordance with cGMP and company policies.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 3 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
• In-depth knowledge of cGMP, ICH guidelines, and other relevant regulatory requirements.
• Experience with batch record review, deviation management, and CAPA systems.
• Strong analytical and problem-solving skills.
• Excellent written and verbal communication skills.
• Proficiency in Microsoft Office Suite.
• Ability to work independently and as part of a team in a fast-paced environment.
• Detail-oriented with a high level of accuracy.
• Experience with quality management software is a plus.
• Familiarity with validation principles for manufacturing processes and equipment.

• Develop and execute detailed, comprehensive, and well-structured test plans and test cases.
• Identify, record, document thoroughly, and track bugs using issue tracking systems.
• Perform thorough regression testing when bugs are resolved.
• Design and execute automation scripts to improve efficiency and coverage.
• Collaborate with development and product management teams to understand requirements and provide early feedback on design and functionality.
• Monitor all aspects of the product during testing phases, ensuring that expected results are achieved.
• Analyze test results and report on defects and their severity.
• Participate in the continuous improvement of QA processes and methodologies.
• Ensure that all testing activities align with industry standards and company quality objectives.
• Provide clear and concise reports on testing progress, risks, and outcomes.
• Stay current with new testing tools and strategies.

• Proven working experience in quality assurance or manual/automated testing.
• Solid knowledge of QA methodologies, tools, and processes.
• Experience with test case management tools and defect tracking systems (e.g., Jira, TestRail).
• Familiarity with automated testing frameworks (e.g., Selenium, Cypress) is a plus.
• Ability to think critically and analytically to identify potential issues.
• Excellent written and verbal communication skills for clear bug reporting and team collaboration.
• Strong organizational skills and the ability to manage multiple tasks effectively in a remote setting.
• A keen eye for detail and a passion for ensuring product quality.
• Self-motivated and able to work independently with minimal supervision.
• Experience in the cleaning and sanitation sector or related industries is advantageous but not essential.

• Review and approve batch manufacturing records and associated documentation.
• Manage deviations, change controls, and CAPA processes.
• Conduct internal audits and support external regulatory inspections.
• Ensure compliance with GMP, GDP, and other relevant quality standards.
• Participate in the validation of processes, equipment, and analytical methods.
• Maintain and improve the company's Quality Management System (QMS).
• Provide QA support to manufacturing and other departments.
• Contribute to the ongoing training and development of quality awareness.

• Degree in Pharmacy, Chemistry, Biology, or a related scientific field, or equivalent experience.
• Proven experience in pharmaceutical quality assurance or quality control.
• In-depth knowledge of GMP, GDP, and regulatory requirements.
• Experience with QMS, deviation management, and CAPA systems.
• Strong analytical and problem-solving skills.
• Excellent attention to detail and organizational abilities.
• Effective communication and interpersonal skills.

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with GMP, GDP, and other relevant regulatory guidelines.
• Conduct internal audits and inspections to assess compliance with quality standards and identify areas for improvement.
• Review and approve batch records, validation documents, and other quality-related documentation.
• Manage deviations, investigations, and CAPA (Corrective and Preventive Actions) processes.
• Participate in external audits by regulatory authorities and customers.
• Provide training to personnel on quality assurance procedures and regulatory requirements.
• Contribute to risk management activities and quality risk assessments.
• Monitor key quality metrics and prepare reports for management.
• Stay up-to-date with evolving regulatory requirements and industry best practices.
• Collaborate with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs, to ensure quality integration.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science discipline.
• Minimum of 3-5 years of experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and relevant regulatory guidelines (e.g., MHRA, FDA, EMA).
• Experience with auditing, deviation management, and CAPA systems.
• Strong analytical and problem-solving skills with excellent attention to detail.
• Proficient in using quality management software and MS Office Suite.
• Excellent written and verbal communication skills.
• Ability to work effectively both independently and as part of a team in a hybrid environment.
• Understanding of pharmaceutical product development and manufacturing processes.