507 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.

**Before you apply to a job, select your language preference from the options available at the top right of this page.**



Explore your next opportunity at a Fortune Global 500 organization. Envision innovative possibilities, experience our rewarding culture, and work with talented teams that help you become better every day. We know what it takes to lead UPS into tomorrowu2014people with a unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams, there are roles ready to cultivate your skills and take you to the next level.



**Job Description:**



Quality Assurance Specialist



Based: Polar Speed Distribution Ltd, Site2, 8 Chartmoor Road, Leighton Buzzard, Bedfordshire, LU7 4WG



Monday to Friday working 40 hours a week



Key Responsibilities:



Supporting the head of QA and RA, QA managers, responsible persons and qualified persons with the implementation and maintenance of the quality management system in accordance with the GMP and GDP guidelines and GPhC, ISO9001 and ISO 13485 standards.



Supporting ongoing compliance with relevant standards, legal requirements, regulations and the PSDL documented policies and procedures.



Promote a positive quality culture within the organisation.



Supporting quality system management reviews, including the preparation of meeting inputs, attendance and presentation at meetings and the management of the meeting outputs.



Supporting regulatory, ISO and client audits, and conducting supplier audits, internal audits and self inspections, including the preparation of responses and CAPA plans.



Preparing draft quality technical agreements for clients and suppliers.



Supporting in the preparation and review of risk assessments for quality risk management and change requests.



Ensuring the effective control of all documentation within the quality management team in line with procedures for the control of documents, physical and electronic records.



Investigation and reporting of incidents including deviations, non conformances, client feedback and customer compliants, including the logging, notification, investigation, reporting and approval of incidents.



Collaborating with the RPs to urgently and accurately perform all operations required during a pharmaceutical call.



Reviewing and logging all MHRA product recall notifications.



Assisting with the implementation and maintenance of company training programs.



Assisting with the monitoring and evaluation trends in warehouse and vehicle temperature conditions to ensure that products and orders are stored and transported in the correct conditions.



Reviewing and approving of records relating to premises and equipment, including temperature records, alarm tests, cleaning logs, pest control reports and calibration certificates.



Completing client quality questionnaires and providing support to clients when qualifying Polar Speed as a supplier.



Participating in the qualification and ongoing management of suppliers, customers and outsourced service providers.



Conduct fortnightly regulatory checks of suspended, cancelled, terminated and revoked licences.



Support with completion of returns forms and management of returns products.



Providing QA oversight quarantined stock, to ensure accuracy in identifying quarantined and released products.



Preparing quality statements requested by clients to confirm product storage conditions.



Preparing and review the documentation packs for the RPI release of imported medicinal products.



Complete the quality control checks required for GMP activities.



Producing and evaluating QA and KPI reports for internal and external customers.



Participating in client meetings to discuss QA related activities, including incident investigations, CAPA, change control and risk assessment.



**Employee Type:**



Permanent



UPS is committed to providing a workplace free of discrimination, harassment, and retaliation.

**Before you apply to a job, select your language preference from the options available at the top right of this page.**



Explore your next opportunity at a Fortune Global 500 organization. Envision innovative possibilities, experience our rewarding culture, and work with talented teams that help you become better every day. We know what it takes to lead UPS into tomorrowu2014people with a unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams, there are roles ready to cultivate your skills and take you to the next level.



**Job Description:**



Quality Assurance Specialist



Based: Polar Speed Distribution Ltd, Site2, 8 Chartmoor Road, Leighton Buzzard, Bedfordshire, LU7 4WG



Monday to Friday working 40 hours a week



Key Responsibilities:



Supporting the head of QA and RA, QA managers, responsible persons and qualified persons with the implementation and maintenance of the quality management system in accordance with the GMP and GDP guidelines and GPhC, ISO9001 and ISO 13485 standards.



Supporting ongoing compliance with relevant standards, legal requirements, regulations and the PSDL documented policies and procedures.



Promote a positive quality culture within the organisation.



Supporting quality system management reviews, including the preparation of meeting inputs, attendance and presentation at meetings and the management of the meeting outputs.



Supporting regulatory, ISO and client audits, and conducting supplier audits, internal audits and self inspections, including the preparation of responses and CAPA plans.



Preparing draft quality technical agreements for clients and suppliers.



Supporting in the preparation and review of risk assessments for quality risk management and change requests.



Ensuring the effective control of all documentation within the quality management team in line with procedures for the control of documents, physical and electronic records.



Investigation and reporting of incidents including deviations, non conformances, client feedback and customer compliants, including the logging, notification, investigation, reporting and approval of incidents.



Collaborating with the RPs to urgently and accurately perform all operations required during a pharmaceutical call.



Reviewing and logging all MHRA product recall notifications.



Assisting with the implementation and maintenance of company training programs.



Assisting with the monitoring and evaluation trends in warehouse and vehicle temperature conditions to ensure that products and orders are stored and transported in the correct conditions.



Reviewing and approving of records relating to premises and equipment, including temperature records, alarm tests, cleaning logs, pest control reports and calibration certificates.



Completing client quality questionnaires and providing support to clients when qualifying Polar Speed as a supplier.



Participating in the qualification and ongoing management of suppliers, customers and outsourced service providers.



Conduct fortnightly regulatory checks of suspended, cancelled, terminated and revoked licences.



Support with completion of returns forms and management of returns products.



Providing QA oversight quarantined stock, to ensure accuracy in identifying quarantined and released products.



Preparing quality statements requested by clients to confirm product storage conditions.



Preparing and review the documentation packs for the RPI release of imported medicinal products.



Complete the quality control checks required for GMP activities.



Producing and evaluating QA and KPI reports for internal and external customers.



Participating in client meetings to discuss QA related activities, including incident investigations, CAPA, change control and risk assessment.



**Employee Type:**



Permanent



UPS is committed to providing a workplace free of discrimination, harassment, and retaliation.

Quality Assurance Specialist
Location: Flexible, with hybrid working and regular travel across the South East and South West
Contract Type: Full time, permanent
Salary: 29,500

About theBusiness
Our client delivers integrated facilities management and accommodation maintenance services as part of a major UK defence contract. Their mission is to ensure safe, efficient, and high-quality services that support operational readiness and the wellbeing of service personnel and their families. They are committed to putting customers and families first, ensuring that every service, whether a reactive repair or a major project is completed safely, on time, and to the highest standard. Their core values of openness, care, agility, and collaboration underpin all aspects of their operations and drive continuous improvement across their services.

Role Overview
The Quality Assurance Specialist will play a key role in maintaining and improving quality standards across a large and complex accommodation contract. Reporting to the Quality Manager, this role involves implementing assurance processes, conducting inspections, analysing performance data, and providing guidance to operational teams and supply chain partners.
This is a highly visible position that requires engagement with internal stakeholders and external partners to embed a culture of quality and compliance. The successful candidate will also contribute to developing best practice, supporting audits, and driving continuous improvement initiatives to ensure contractual and regulatory obligations are consistently met.

Key Responsibilities

• Carry out site inspections and assurance sampling to monitor compliance with contractual, statutory, and quality management requirements
• Support the implementation and review of the Quality Management Plan, ensuring alignment with ISO 9001:2015 standards
• Identify and record non-conformances, investigate root causes, and ensure timely completion of corrective actions
• Analyse data from audits, inspections, and customer feedback to identify trends and recommend improvement actions
• Prepare accurate and detailed quality reports for senior management and maintain all quality records within the CAFM system
• Deliver training and briefing sessions to operational teams and supply chain partners on quality assurance processes and standards
• Promote continuous improvement initiatives, contributing to the development of best practice and efficiency gains across the contract
• Support audit activities, both internal and external, by providing evidence and ensuring compliance with audit requirements
• Act as a key contact for quality-related queries, working collaboratively with operational teams, clients, and subcontractors
• Maintain up-to-date knowledge of industry standards and participate in professional development to ensure ongoing competence

Essential Skills and Experience

• Strong understanding of quality assurance principles and processes
• Ability to analyse data and present findings in a clear and actionable format
• Experience delivering training and providing professional guidance
• Proficiency in Microsoft Office applications, particularly Excel, for reporting and analysis
• Full UK driving licence and flexibility to travel extensively across the South East and South West
• Excellent organisational skills with the ability to manage multiple priorities and meet deadlines

Desirable Skills and Qualifications

• Experience within the facilities management or construction sector
• ISO 9001:2015 Internal or Lead Auditor qualification
• Knowledge of Lean Six Sigma or other process improvement methodologies
• Practitioner or Chartered membership of the Chartered Quality Institute (CQI)
• Advanced Excel skills and experience using CAFM or quality management software

What the Role Offers
This is an excellent opportunity to influence quality standards within a high-profile and nationally significant contract. The role combines operational engagement with strategic improvement, offering variety, autonomy, and the chance to make a real difference to service delivery

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.

**Before you apply to a job, select your language preference from the options available at the top right of this page.**
Explore your next opportunity at a Fortune Global 500 organization. Envision innovative possibilities, experience our rewarding culture, and work with talented teams that help you become better every day. We know what it takes to lead UPS into tomorrow-people with a unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams, there are roles ready to cultivate your skills and take you to the next level.
**Job Description:**
Quality Assurance Specialist
Based: Polar Speed Distribution Ltd, Site2, 8 Chartmoor Road, Leighton Buzzard, Bedfordshire, LU7 4WG
Monday to Friday working 40 hours a week
Key Responsibilities:
Supporting the head of QA and RA, QA managers, responsible persons and qualified persons with the implementation and maintenance of the quality management system in accordance with the GMP and GDP guidelines and GPhC, ISO9001 and ISO 13485 standards.
Supporting ongoing compliance with relevant standards, legal requirements, regulations and the PSDL documented policies and procedures.
Promote a positive quality culture within the organisation.
Supporting quality system management reviews, including the preparation of meeting inputs, attendance and presentation at meetings and the management of the meeting outputs.
Supporting regulatory, ISO and client audits, and conducting supplier audits, internal audits and self inspections, including the preparation of responses and CAPA plans.
Preparing draft quality technical agreements for clients and suppliers.
Supporting in the preparation and review of risk assessments for quality risk management and change requests.
Ensuring the effective control of all documentation within the quality management team in line with procedures for the control of documents, physical and electronic records.
Investigation and reporting of incidents including deviations, non conformances, client feedback and customer compliants, including the logging, notification, investigation, reporting and approval of incidents.
Collaborating with the RPs to urgently and accurately perform all operations required during a pharmaceutical call.
Reviewing and logging all MHRA product recall notifications.
Assisting with the implementation and maintenance of company training programs.
Assisting with the monitoring and evaluation trends in warehouse and vehicle temperature conditions to ensure that products and orders are stored and transported in the correct conditions.
Reviewing and approving of records relating to premises and equipment, including temperature records, alarm tests, cleaning logs, pest control reports and calibration certificates.
Completing client quality questionnaires and providing support to clients when qualifying Polar Speed as a supplier.
Participating in the qualification and ongoing management of suppliers, customers and outsourced service providers.
Conduct fortnightly regulatory checks of suspended, cancelled, terminated and revoked licences.
Support with completion of returns forms and management of returns products.
Providing QA oversight quarantined stock, to ensure accuracy in identifying quarantined and released products.
Preparing quality statements requested by clients to confirm product storage conditions.
Preparing and review the documentation packs for the RPI release of imported medicinal products.
Complete the quality control checks required for GMP activities.
Producing and evaluating QA and KPI reports for internal and external customers.
Participating in client meetings to discuss QA related activities, including incident investigations, CAPA, change control and risk assessment.
**Employee Type:**
Permanent
UPS is committed to providing a workplace free of discrimination, harassment, and retaliation.

I’m currently working with a leading university on the search for a quality assurance consultant on a 2-month contract, working remotely. This role requires you to scope their current quality assurance processes, lead a complete refresh, and leverage your experience working with their partners. Experience Required: Proven background in Higher Education Quality Assurance, including an understanding of regulatory frameworks and external review bodies (e.g., QAA, OfS). Experience rewriting and implementing Quality Assurance processes across an entire institution or department. Demonstrable experience of successful stakeholder management at all levels, from academic staff and senior leadership to external partners. Direct experience leading a complete refresh or review of quality assurance systems, including the ability to scope, plan, and execute a project from start to finish. In-depth knowledge of academic partnership management, with a focus on ensuring quality and compliance across all collaborative provision. If you are interested in please apply now!

A leading Pharmaceutical company in the Berkshire area, is seeking a dedicated QA Specialist. As the QA Specialist, you will play a crucial role in ensuring the timely establishment and maintenance of customer Quality Agreements (QAA) between our client and its customers. This role offers a balanced work arrangement with 3 days onsite and 2 days from home, providing flexibility and is an initial 12 month contract. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QA Specialist will be varied however the key duties and responsibilities are as follows: 1. As the QA Specialist, you will act as the primary point of contact for Quality Agreements, representing the company in negotiations and ensuring consistency between internal processes and commitments in QAAs. 2. As the QA Specialist, you will set up and manage an efficient system to track the completion status of QAAs, monitor requirements for periodic review, and initiate reviews as needed. 3. As the QA Specialist, you will participate in global QAA SOP revision working groups, improve existing tracking tools, and create new solutions for QAA-related document life cycles. 4. As the QA Specialist, you will provide training on the QAA structure and content to functional teams within the company. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the QA Specialist we are looking to identify the following on your profile and past history: 1. Relevant degree in a science-related discipline. 2. Extensive industry experience within a GMP-regulated pharmaceutical environment, ideally in biologics or biopharmaceuticals, and/or relevant QA experience. 3. A working knowledge and practical experience with risk-based decision-making, problem-solving, and accurate data entry skills. Key Words: Quality Agreements Specialist / QA Specialist / Quality Assurance Specialist / QAA / pharmaceutical industry / GMP-regulated / biologics / biopharmaceuticals / risk-based decision-making / data entry / customer relations / SOP revision / document life cycle Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

We have an opportunity to join our Quality Assurance team based at our Glasgow site in the role of Quality Specialist. 12 month FTC (Mat Cover). This is a technical position, with responsibility for providing support functions for the QA group and ensuring this work is performed in an organised and timely manner. Additionally, performs administrative and technical Quality Assurance duties, whilst adhering to GMP, COSHH and Health and Safety regulations. Quality Assurance operates as a support function for site, ensuring that all activities adhere to the requirements of the Quality Management System and that the site operates in compliance with current GMP. All work is performed within the Glasgow facility and operates to ensure that sterile products are manufactured to GMP in a consistent manner Responsibilities include but not limited: Documents and reports of all work in adherence with GMP and departmental procedures. Performs batch review within the designated timelines described in departmental KPI. Authors and reviews SOPs. Reviews change controls, CAPAs and deviations. Provides feedback / corrections to authors and escalates concerns to QA Manager where necessary. Raise CAPA, approve category CA/PA and review for completion CAPA and support the completion of actions through liaison with other departments. Represent Quality Assurance in continuous improvement projects ensuring that change is performed in accordance with GMP, site procedures and industry regulations and guidelines. Identifies and performs personal development in line with agreed and documented annual goals including successful completion of internal and external training course. Supports the completion of administration tasks associated with of supplier certification. Acts as a support to client audits and regulatory inspections, helping with technical support to the audit team and responding to requests for documentation and information. Works to a schedule as defined by the QA Manager. Conducts self-inspection’s / audits to ensure compliance with Quality Management System procedures and GMP regulations. Ensuring that a timely and effective communication and escalation of quality issues to the appropriate levels of management. Carries out site internal audits and identifies areas of GMP improvement during their daily duties, and participate in client projects as a QA representative. Carries out training for QMS activities as defined by line management. Utilise Curia Global training platforms. Actively participle in achieving the QA/Quality KPI’s and participate in the QA on-call rotation as required. Responsible for identifying corrections necessary to batch records or other QMS documents and making suggestions to operational or laboratory functions to enhance GMP compliance. Responsible for reviewing and progressing Minor/Major category deviations and CAPA in reasonable time frames. Responsible for providing advice based on GMP and scientific rational to departments when designated the QA individual ‘On call’ or escalating to QA Manager, where appropriate. Skills and Qualifications: Hold a Science related degree qualification Wide breadth and depth of knowledge and understanding in regulatory requirements and GMP, ICH, COSHH etc. Knowledge and experience of UK / EU / US GMP and Quality Assurance. Ideally Experience in an aseptic manufacturing environment. Prioritise tasks and meet deadlines. Proven experience within a similar Quality environment is advantageous Hours: 8-hour shift including breaks, with a flexible starting and finish time between 7:30am and 6:30pm, Monday to Friday (overtime and on call available) Curia (Scotland) Limited is committed to fostering a diverse and inclusive workplace where all perspectives are valued and respected. We proudly support equal opportunity and are an affirmative-action employer, welcoming applications from all qualified individuals. We consider all applicants for employment without regard to age, race, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, veteran status, or any other protected status.