What Jobs are available for Quality Control Specialists in the United Kingdom?

• Oversee and perform a wide range of quality control tests on raw materials, in-process samples, and finished products using various analytical techniques.
• Develop, validate, and implement new testing methods and procedures according to regulatory guidelines (e.g., GMP, ICH).
• Train and mentor junior QC analysts, providing guidance on testing protocols, equipment usage, and data interpretation.
• Review and approve analytical test results, ensuring accuracy, completeness, and compliance with specifications.
• Manage and maintain laboratory equipment, including calibration, preventative maintenance, and troubleshooting.
• Investigate out-of-specification (OOS) results and deviations, determining root causes and implementing corrective and preventative actions (CAPAs).
• Participate in internal and external audits, ensuring the QC laboratory is inspection-ready.
• Maintain accurate and detailed laboratory records, including raw data, reports, and certificates of analysis.
• Contribute to the continuous improvement of QC processes and systems.
• Liaise with R&D, production, and regulatory affairs departments on quality-related matters.
• Ensure compliance with all health, safety, and environmental regulations within the laboratory.

• Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related scientific discipline.
• Minimum of 5 years of experience in a pharmaceutical Quality Control laboratory setting.
• Extensive hands-on experience with analytical techniques such as HPLC, GC, UV-Vis spectroscopy, FTIR, and dissolution testing.
• Thorough understanding of Good Manufacturing Practices (GMP), regulatory guidelines, and quality management systems.
• Proven ability to develop and validate analytical methods.
• Experience in investigating OOS results and deviations.
• Strong leadership, problem-solving, and decision-making skills.
• Excellent attention to detail and organizational abilities.
• Proficiency in using laboratory information management systems (LIMS) and standard laboratory software.
• Effective communication and interpersonal skills for team collaboration and interdepartmental liaison.

• Evaluate and audit existing sanitation procedures and protocols.
• Develop and update sanitation guidelines and best practices.
• Conduct remote assessments of cleaning and hygiene standards.
• Analyze data related to sanitation effectiveness and compliance.
• Provide expert recommendations for improving hygiene and safety measures.
• Ensure adherence to relevant industry regulations and standards.
• Prepare detailed reports and present findings to stakeholders.
• Collaborate with teams to implement quality improvement initiatives.
• Stay informed about emerging trends and technologies in sanitation.
• Maintain accurate records of all quality control activities.

• Proven experience in quality control, with a focus on sanitation, hygiene, or environmental health.
• Strong understanding of sanitation principles and best practices.
• Excellent analytical, problem-solving, and critical thinking skills.
• Proficiency in data analysis and report writing.
• Ability to work independently and manage time effectively in a remote setting.
• Strong communication and interpersonal skills.
• Familiarity with relevant industry regulations and compliance standards.
• Detail-oriented with a high level of accuracy.
• Experience with quality management systems is advantageous.
• Relevant certifications in sanitation or quality management are a plus.

• Develop, implement, and maintain comprehensive sanitation and hygiene quality control programs.
• Conduct remote inspections and audits of cleaning procedures and standards using provided checklists and virtual tools.
• Analyze inspection data and identify areas for improvement or non-compliance.
• Develop and deliver training materials on sanitation best practices to cleaning staff and relevant personnel.
• Stay up-to-date with industry regulations, best practices, and emerging trends in sanitation and infection control.
• Investigate and report on sanitation-related incidents or complaints.
• Collaborate with facility management and operational teams to ensure effective implementation of quality standards.
• Prepare detailed reports on quality control findings, trends, and recommendations for corrective actions.
• Manage and maintain records of all quality control activities, including inspection results and training logs.
• Advise on the selection and proper use of cleaning chemicals and equipment.
• Contribute to the development and refinement of standard operating procedures (SOPs) for sanitation.
• Ensure compliance with health, safety, and environmental regulations.
• Perform root cause analysis for any quality deviations and recommend preventive measures.
• Maintain a high level of accuracy and attention to detail in all quality assurance activities.
• Communicate effectively with team members and stakeholders regarding quality standards and improvements.

• Proven experience in quality control, sanitation management, hygiene assessment, or a related field.
• Strong knowledge of cleaning science, disinfection protocols, and infection control principles.
• Familiarity with relevant health, safety, and environmental regulations.
• Experience in developing and implementing quality management systems or SOPs.
• Excellent observational skills and a meticulous attention to detail.
• Strong analytical and problem-solving abilities.
• Proficiency in using digital tools for documentation, data entry, and virtual communication.
• Ability to work independently and manage time effectively in a remote setting.
• Excellent written and verbal communication skills.
• Ability to interpret and apply complex guidelines and regulations.
• Experience in conducting audits or inspections, ideally remotely.
• A proactive approach to identifying and addressing potential issues.
• Certification in a relevant field (e.g., CMI, ISSA CWS) is a plus.
• A dedicated home office setup with reliable internet connectivity is required.

• Perform incoming material inspections, in-process checks, and finished product testing according to established protocols.
• Conduct physical, chemical, and microbiological testing of cosmetic products and raw materials.
• Utilise laboratory equipment and instruments to perform analyses, ensuring calibration and maintenance.
• Document all quality control findings, results, and deviations accurately in compliance with GMP (Good Manufacturing Practices).
• Identify and report any product or process non-conformities to management.
• Assist in the investigation of quality complaints and deviations.
• Ensure adherence to all relevant industry regulations and standards (e.g., ISO 22716, FDA).
• Maintain a clean and organised laboratory environment.
• Participate in internal quality audits and continuous improvement initiatives.
• Collaborate with production, R&D, and regulatory teams to address quality concerns.

• Bachelor's degree in Chemistry, Biology, Pharmacy, or a related scientific discipline.
• Minimum of 2-3 years of experience in Quality Control or Quality Assurance, preferably within the cosmetic, personal care, or pharmaceutical industry.
• Familiarity with Good Manufacturing Practices (GMP) and quality control procedures.
• Experience with common laboratory testing techniques and equipment.
• Strong attention to detail and accuracy in record-keeping.
• Good understanding of cosmetic product ingredients and formulation basics.
• Basic knowledge of relevant regulatory requirements for cosmetics.
• Effective communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficiency in Microsoft Office Suite.

• Develop and refine comprehensive quality control plans and standard operating procedures (SOPs) for cleaning and sanitation services.
• Conduct remote audits and assessments of cleaning processes and documentation at various sites.
• Analyse data from inspections, audits, and performance metrics to identify trends and areas for improvement.
• Provide expert guidance and training to site-based teams on best practices in cleaning and sanitation.
• Investigate and resolve quality-related issues and customer complaints, implementing corrective and preventive actions.
• Stay informed about relevant regulations, industry standards (e.g., BICS, ISSA), and emerging best practices in sanitation and hygiene.
• Prepare detailed reports on quality performance, audit findings, and improvement initiatives for senior management.
• Collaborate with operational teams to ensure effective implementation of quality standards.
• Develop and manage quality-related documentation and records.
• Contribute to the continuous improvement of the organization's sanitation strategies.

• Significant experience in quality control, quality assurance, or a similar role within the cleaning, sanitation, or facilities management industry.
• In-depth knowledge of cleaning techniques, sanitation principles, and health & safety regulations.
• Proven ability to develop and implement robust quality management systems.
• Strong analytical and problem-solving skills, with meticulous attention to detail.
• Excellent written and verbal communication skills, capable of delivering clear instructions and constructive feedback remotely.
• Proficiency in data analysis and reporting tools.
• Experience with audit procedures and documentation.
• Relevant certifications in sanitation, hygiene, or quality management (e.g., CQIA, ISO 9001 knowledge) are a plus.
• Ability to work independently, manage time effectively, and maintain high levels of productivity in a remote setting.
• A bachelor's degree in a relevant field or equivalent practical experience.

A fast-growing electrical engineering business based near Manchester Airport is seeking an experienced Quality Control Specialist for a 6-month interim role, with the potential for a permanent contract thereafter.

The organisation is currently transitioning from ISO 9001 to ISO 14001 and has ambitious plans to upgrade its Quality Assurance systems to AS9100D as part of its ongoing growth and commitment to excellence.

THE JOB

The primary purpose of this interim role is to support the implementation and documentation of ISO 14001 and AS9100D, while assisting with the ongoing maintenance and improvement of the Quality Management System (QMS).

Working closely with the Quality Control Director, you’ll contribute to a strategically important programme focused on:

• Updating the existing ISO 9001 framework and implementing ISO 14001 by March 2026
• Supporting AS9100D implementation, a key milestone in the company’s growth strategy

This hands-on role will involve reviewing and refining QC processes, collaborating with consultants, production, and procurement teams, and ensuring compliance with the highest quality and environmental standards.

Your day-to-day duties will include:

• Ensuring products and processes comply with organisational objectives, regulatory standards, and quality assurance requirements
• Conducting audits, managing non-conformance reports, and maintaining key documentation and records, including suppliers, assets, and COSHH assessments
• Continuously reviewing and updating processes, change notifications, and business risk analyses to drive quality improvements
• Monitoring, reporting, and analysing Quality KPIs to support performance objectives
• Undertaking ad hoc activities to meet evolving business and compliance needs

THE PERSON

We’re looking for someone with a strong background in quality assurance and a proactive, detail-driven approach.

Essential/Desirable Skills & Experience:

• Knowledge of COSHH assessments
• Experience in electronic assembly (preferred)
• ONC/HNC qualification within electronics or a related discipline (preferred)
• Minimum 3–5 years’ experience working with ISO 9001 (other standards advantageous)
• Strong attention to detail and excellent organisational skills
• Clear and confident communication abilities
• Ability to work effectively under pressure and meet deadlines
• 5 GCSEs (Grade 5/C or above) desirable

THE BENEFITS

• Working hours Mon – Fri 9am – 5pm (37.5hrs)
• 6-month interim contract (potential for permanent role)
• 100% office-based position
• Free onsite parking
• 25 days annual leave (pro-rata)
• Opportunity to make a tangible impact on a business during a key transformation phase

If you’re passionate about continuous improvement, quality excellence, and helping shape a growing company’s future, we’d love to hear from you, so please apply today!

A fast-growing electrical engineering business based near Manchester Airport is seeking an experienced Quality Control Specialist for a 6-month interim role, with the potential for a permanent contract thereafter.

The organisation is currently transitioning from ISO 9001 to ISO 14001 and has ambitious plans to upgrade its Quality Assurance systems to AS9100D as part of its ongoing growth and commitment to excellence.

THE JOB

The primary purpose of this interim role is to support the implementation and documentation of ISO 14001 and AS9100D, while assisting with the ongoing maintenance and improvement of the Quality Management System (QMS).

Working closely with the Quality Control Director, you’ll contribute to a strategically important programme focused on:

• Updating the existing ISO 9001 framework and implementing ISO 14001 by March 2026
• Supporting AS9100D implementation, a key milestone in the company’s growth strategy

This hands-on role will involve reviewing and refining QC processes, collaborating with consultants, production, and procurement teams, and ensuring compliance with the highest quality and environmental standards.

Your day-to-day duties will include:

• Ensuring products and processes comply with organisational objectives, regulatory standards, and quality assurance requirements
• Conducting audits, managing non-conformance reports, and maintaining key documentation and records, including suppliers, assets, and COSHH assessments
• Continuously reviewing and updating processes, change notifications, and business risk analyses to drive quality improvements
• Monitoring, reporting, and analysing Quality KPIs to support performance objectives
• Undertaking ad hoc activities to meet evolving business and compliance needs

THE PERSON

We’re looking for someone with a strong background in quality assurance and a proactive, detail-driven approach.

Essential/Desirable Skills & Experience:

• Knowledge of COSHH assessments
• Experience in electronic assembly (preferred)
• ONC/HNC qualification within electronics or a related discipline (preferred)
• Minimum 3–5 years’ experience working with ISO 9001 (other standards advantageous)
• Strong attention to detail and excellent organisational skills
• Clear and confident communication abilities
• Ability to work effectively under pressure and meet deadlines
• 5 GCSEs (Grade 5/C or above) desirable

THE BENEFITS

• Working hours Mon – Fri 9am – 5pm (37.5hrs)
• 6-month interim contract (potential for permanent role)
• 100% office-based position
• Free onsite parking
• 25 days annual leave (pro-rata)
• Opportunity to make a tangible impact on a business during a key transformation phase

If you’re passionate about continuous improvement, quality excellence, and helping shape a growing company’s future, we’d love to hear from you, so please apply today!

Ready to elevate your career with a top-tier steel fabrication leader?

We're expanding our team in Thirsk and looking for a skilled QA/QC Engineer to help drive excellence across major industries like Petrochemical, Pharmaceutical, and Nuclear. Join us on our exciting journey of growth and innovation, where you'll benefit from robust career development opportunities, clear progression paths , and the chance to shape the future of engineering excellence.

Who this job suits:

This role is ideal for an experienced Quality Engineer with a meticulous eye for detail, analytical skills, and prior exposure to large, complex, multi-disciplined projects in regulated environments. Your knowledge of Welding, ISO 3834 & EN 1090 will be high advantageous.

Key Responsibilities:

• Liaise with internal and external stakeholders to ensure project inspections and technical requirements are met.
• Ensure compliance to ISO 3834, EN 1090, ISO 9001.
• Collate and analyse data, support audits, and liaise with clients.
• Utilize extensive hands-on experience in Quality Management Systems and Principles.
• Interpret and accept contract NDT reports on behalf of the business.

Skills and Experience:

• CSWIP 3.1 certified
• Auditor certified
• PCN Level 2 certified
• Time-served apprenticeship, HNC, HND or equivalent
• Knowledge of ISO 3834 (welding inspection) and/or EN 1090 advantageous
• Experience with LTQRs advantageous

Location : Thirsk

Contract: 12 month FTC - Fixed Term Contract

Salary: circa £40k - £45k (dependent on experience)

Hours: 37.5 hours per week. 07.45 – 16:45 Monday - Thursday, 7.30 - 12:00 Friday.

Benefits: Pension, Medical Cover, 25 days + BH, Cycle to Work, Save as you earn scheme, Counselling & Support, further Benefit schemes.

APPLY NOW!

Contact Jacob Golding for further details – –