50 Quality Assurance jobs in Bradford

Thrive Personnel Ltd are looking to recruit an experienced QA Manager to join our client a leading food production business based in Pontefract West Yorkshire.

The Quality Assurance (QA) Manager is responsible for overseeing and managing all aspects of the food safety and quality programs within the food production facility. This role ensures that products meet established quality standards, comply with regulatory requirements, and satisfy customer expectations. The QA Manager leads a team of QA professionals, implements quality control procedures, and drives continuous improvement initiatives to maintain the highest levels of product quality and safety.

Responsibilities:

Develop, implement, and maintain the company's food safety and quality assurance programs, including HACCP, GMPs, and other relevant standards.

Lead and manage a team of QA professionals, providing guidance, training, and support to ensure effective performance and professional development.

Establish and maintain quality control procedures for incoming raw materials, in-process production, and finished products.

Conduct regular audits and inspections of the facility, processes, and equipment to identify potential hazards and ensure compliance with food safety regulations.

Investigate and resolve quality issues, customer complaints, and non-conformances, implementing corrective and preventive actions to prevent recurrence.

Monitor and analyze quality data, identify trends, and implement strategies to improve product quality and process efficiency.

Collaborate with other departments, such as production, sanitation, and maintenance, to ensure alignment of quality and food safety objectives.

Stay up-to-date on industry trends, regulatory requirements, and scientific advancements related to food safety and quality assurance.

Serve as the primary point of contact for regulatory agencies, customers, and third-party auditors regarding food safety and quality matters.

Manage the facility's laboratory operations, including testing, analysis, and equipment maintenance.

Develop and manage the QA budget, ensuring efficient allocation of resources to support quality and food safety initiatives.

Qualifications:

5+ years of experience in quality assurance within the food production industry, with at least 2 years in a managerial role.

In-depth knowledge of food safety regulations, HACCP principles, GMPs, and other relevant standards.

Strong leadership and management skills, with the ability to motivate and develop a team of QA professionals.

Excellent analytical and problem-solving skills, with the ability to identify and resolve quality issues effectively.

Effective communication and interpersonal skills, with the ability to collaborate with cross-functional teams and external stakeholders.

Experience with laboratory operations, including testing, analysis, and equipment maintenance.

Certified Quality Manager (CQM) or other relevant certifications preferred.

Proficiency in Microsoft Office Suite and other relevant software applications.

This is a permanent role with scope for progression and development.

• Oversee and manage the company's Quality Management System (QMS) to ensure compliance with GMP and other applicable regulations.
• Develop, implement, and maintain standard operating procedures (SOPs) and quality policies.
• Lead and participate in internal and external audits (regulatory bodies, suppliers, customers).
• Manage deviation investigations, root cause analysis, and the implementation of CAPAs.
• Review and approve batch records, validation documents, and other critical quality documentation.
• Ensure all pharmaceutical products meet stringent quality and safety standards before release.
• Lead, train, and mentor the Quality Assurance team, fostering a high-performance culture.
• Collaborate with other departments (e.g., Production, R&D, Regulatory Affairs) to resolve quality issues and drive continuous improvement.
• Monitor key quality metrics and prepare regular quality reports for senior management.
• Stay current with evolving pharmaceutical regulations and industry best practices.
• Manage supplier qualification and ongoing quality monitoring.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science discipline.
• Minimum of 6 years of progressive experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, regulatory requirements (MHRA, FDA), and quality management systems.
• Proven experience in managing audits, deviations, and CAPA processes.
• Strong leadership and team management skills.
• Excellent analytical, problem-solving, and decision-making abilities.
• Exceptional attention to detail and commitment to accuracy.
• Strong communication and interpersonal skills, with the ability to effectively interact with all levels of the organization and external stakeholders.
• Proficiency in relevant quality management software and tools.
• Experience working within a regulated manufacturing environment.

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with cGMP and other relevant regulatory standards.
• Lead and manage QA personnel, providing guidance and fostering a culture of quality excellence.
• Oversee all aspects of internal and external audits, including preparation, execution, and follow-up actions.
• Manage deviation investigations, CAPA (Corrective and Preventive Actions) implementation, and change control processes.
• Ensure compliance with regulatory requirements from agencies such as the MHRA, FDA, and EMA.
• Review and approve critical quality documents, including batch records, validation protocols, and SOPs.
• Conduct risk assessments and implement risk mitigation strategies.
• Provide quality assurance training to relevant personnel.
• Collaborate with other departments, including manufacturing, R&D, and regulatory affairs, to ensure quality is integrated throughout the product lifecycle.
• Monitor key quality metrics and report on the effectiveness of the QMS to senior management.
• Stay abreast of evolving regulatory landscapes and industry best practices.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 8 years of experience in pharmaceutical quality assurance, with at least 3 years in a management or supervisory role.
• In-depth knowledge of cGMP, ICH guidelines, and global pharmaceutical regulations.
• Strong understanding of pharmaceutical manufacturing processes and quality control.
• Proven experience in managing audits, investigations, and regulatory inspections.
• Excellent leadership, communication, and problem-solving skills.
• Ability to work effectively in a hybrid environment, balancing remote and on-site responsibilities.
• Experience with electronic quality management systems (eQMS) is highly desirable.
• Detail-oriented with a strong commitment to accuracy and compliance.

• Develop, implement, and maintain quality assurance procedures and protocols across all production lines.
• Conduct regular inspections and audits of raw materials, in-process production, and finished goods to ensure compliance with quality standards.
• Utilize statistical methods and tools to monitor, analyse, and improve product quality and process efficiency.
• Investigate product non-conformances, identify root causes, and implement corrective and preventive actions (CAPA).
• Collaborate closely with production, engineering, and R&D teams to resolve quality issues and drive continuous improvement initiatives.
• Manage the calibration and maintenance of quality control equipment and instrumentation.
• Prepare detailed quality reports, including trend analysis, inspection results, and non-conformance summaries for management review.
• Ensure adherence to relevant industry regulations and certifications (e.g., ISO 9001).
• Train production and quality personnel on quality standards, procedures, and best practices.
• Lead and participate in cross-functional teams focused on process improvement and defect reduction.
• Maintain accurate and organised quality documentation, records, and databases.
• Stay updated on new quality assurance technologies, methodologies, and industry best practices.
• Conduct supplier quality audits and work with suppliers to improve material quality.

• Bachelor's degree in Engineering, Science, or a related technical field.
• Minimum of 5 years of experience in a Quality Assurance or Quality Control role within a manufacturing environment.
• Proven experience with Quality Management Systems (e.g., ISO 9001, IATF 16949).
• Strong knowledge of statistical process control (SPC), Six Sigma, or Lean Manufacturing principles.
• Proficiency in using various quality control tools and equipment.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong understanding of manufacturing processes and product development lifecycles.
• Effective communication and interpersonal skills, with the ability to collaborate across departments.
• Detail-oriented with a commitment to accuracy and thoroughness.
• Experience in conducting internal and external audits is highly desirable.
• Proficiency in relevant software, including ERP systems and quality management software.

• Proven experience in a Quality Assurance or Quality Control role within manufacturing.
• Strong understanding of quality management systems (e.g., ISO 9001).
• Proficiency in performing various inspections and testing procedures.
• Experience with calibration of testing equipment.
• Knowledge of statistical process control (SPC) techniques.
• Excellent analytical and problem-solving skills.
• Strong attention to detail and accuracy.
• Good communication and interpersonal skills.
• Ability to interpret technical specifications and standards.
• Experience with root cause analysis and corrective action implementation.
• Formal qualification in Quality Assurance is a plus.

• Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with GMP and relevant regulatory guidelines.
• Conduct internal audits of manufacturing processes, documentation, and quality control procedures to ensure compliance.
• Participate in external audits and regulatory inspections by health authorities (e.g., MHRA, FDA).
• Review and approve batch records, validation protocols, and technical reports.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
• Manage change control processes, ensuring all changes are assessed for regulatory impact.
• Train personnel on GMP requirements and quality procedures.
• Contribute to the qualification and validation of equipment and processes.
• Stay up-to-date with evolving regulatory landscapes and industry best practices.
• Prepare quality metrics reports for management review.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 5 years of experience in Quality Assurance within the pharmaceutical industry.
• Thorough understanding of Good Manufacturing Practices (GMP) and relevant regulatory requirements (e.g., ICH, FDA, EMA).
• Experience in conducting and participating in audits.
• Strong knowledge of QMS principles, deviation management, change control, and CAPA systems.
• Excellent analytical and problem-solving skills with a high degree of accuracy.
• Proficiency in documentation review and batch record evaluation.
• Strong written and verbal communication skills.
• Ability to work independently and as part of a team in a fast-paced environment.
• Experience with sterile manufacturing or specific dosage forms is a plus.

• Develop, implement, and maintain robust Quality Management Systems (QMS) in accordance with GMP, ISO, and other relevant regulatory guidelines.
• Oversee quality assurance activities for drug development, manufacturing, and release processes.
• Conduct internal and external audits of suppliers, contract manufacturers, and internal operations.
• Manage the deviation, CAPA (Corrective and Preventive Actions), and change control systems.
• Review and approve critical quality documents, including validation protocols, batch records, and SOPs.
• Lead regulatory inspections and respond to queries from health authorities (e.g., MHRA, FDA, EMA).
• Provide quality assurance training and guidance to staff across different departments.
• Monitor quality metrics and KPIs, reporting on the performance of the QMS to senior management.
• Contribute to risk management activities and ensure potential quality issues are proactively addressed.
• Stay informed about evolving regulatory requirements and industry best practices.
• Participate in product lifecycle management and new product introduction quality oversight.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• Minimum of 7 years of experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of GMP regulations and guidelines (e.g., ICH Q7, 21 CFR Part 210/211).
• Proven experience in managing QMS, conducting audits, and leading regulatory inspections.
• Strong understanding of pharmaceutical manufacturing processes, analytical testing, and validation principles.
• Excellent analytical, problem-solving, and decision-making skills.
• Exceptional written and verbal communication skills, with the ability to present complex information clearly.
• Strong leadership and interpersonal skills, with the ability to influence and collaborate effectively.
• Experience with Quality Risk Management (QRM) principles.
• Proficiency in quality management software and standard office applications.

• Develop and execute comprehensive test strategies, plans, and cases.
• Conduct manual and automated testing of software applications.
• Identify, document, and track software defects and inconsistencies.
• Perform root cause analysis for identified issues.
• Collaborate with development and product teams to ensure product quality.
• Contribute to the enhancement of QA processes and methodologies.
• Automate test scripts to improve testing efficiency.
• Mentor and guide junior QA team members.
• Participate in agile development ceremonies and provide QA insights.
• Ensure compliance with quality standards and best practices.

• Proven experience as a Senior QA Analyst or similar role.
• Strong understanding of software QA methodologies and tools.
• Proficiency in test automation frameworks and scripting languages (e.g., Selenium, Cypress, JavaScript).
• Experience with bug tracking systems (e.g., Jira) and test management tools.
• Familiarity with Agile/Scrum development processes.
• Excellent analytical and problem-solving skills.
• Strong written and verbal communication skills, essential for remote collaboration.
• Ability to work independently and manage time effectively in a remote environment.
• Experience with performance and security testing is a plus.
• Bachelor's degree in Computer Science or a related field, or equivalent practical experience.

• Developing, implementing, and maintaining the company's Quality Management System (QMS) in accordance with relevant ISO standards and industry-specific requirements.
• Leading and mentoring the Quality Assurance team, providing guidance and support to ensure effective performance.
• Designing and executing quality control plans for raw materials, in-process production, and finished goods.
• Conducting internal and external audits to ensure compliance with quality standards and regulatory requirements.
• Investigating quality deviations, identifying root causes, and implementing corrective and preventative actions (CAPA).
• Developing and analysing quality metrics and key performance indicators (KPIs) to monitor and report on quality performance.
• Collaborating with R&D, production, and engineering teams to ensure quality is built into new products and processes.
• Managing customer complaints related to product quality, ensuring timely resolution and customer satisfaction.
• Implementing statistical process control (SPC) techniques to monitor and control manufacturing processes.
• Driving a culture of quality excellence throughout the organisation.