530 Medical Quality Assurance jobs in the United Kingdom

• Develop, implement, and manage the Quality Management System (QMS) in accordance with relevant medical device regulations (e.g., ISO 13485, FDA 21 CFR Part 820).
• Lead and conduct internal and external audits to ensure compliance and identify areas for improvement.
• Manage the CAPA (Corrective and Preventive Actions) process, including investigation, root cause analysis, and implementation of effective corrective actions.
• Review and approve product development documentation, including design controls, risk management files, and validation reports.
• Develop and execute quality control procedures and test methods for incoming materials, in-process production, and finished goods.
• Monitor manufacturing processes to ensure adherence to established quality standards and procedures.
• Analyze quality data and trends, generating reports and making recommendations for process improvements.
• Support regulatory submissions and inspections by health authorities.
• Provide training and guidance to personnel on quality standards and procedures.
• Collaborate with cross-functional teams to resolve quality issues and implement robust solutions.
• Stay current with evolving regulations and industry best practices in medical device quality assurance.

• Bachelor's degree in Engineering, Life Sciences, or a related technical field.
• Minimum of 5-7 years of experience in Quality Assurance within the medical device industry.
• In-depth knowledge of ISO 13485 and FDA QSR (21 CFR Part 820).
• Proven experience with QMS implementation, maintenance, and auditing.
• Strong understanding of design controls, risk management (ISO 14971), and statistical process control (SPC).
• Experience with CAPA management and root cause analysis techniques.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong written and verbal communication skills.
• Ability to work independently and manage multiple priorities in a remote environment.
• Relevant certifications (e.g., CQE, CQA) are highly desirable.

• Lead the development, implementation, and maintenance of the Quality Management System (QMS) in compliance with ISO 13485, FDA 21 CFR Part 820, and other relevant regulations.
• Manage and mentor the Quality Assurance team, providing guidance and fostering professional development.
• Oversee all QA activities, including document control, change control, CAPA management, and internal audits.
• Conduct and manage internal and external audits (regulatory bodies, Notified Bodies, customer audits).
• Ensure product compliance with all applicable quality standards and regulatory requirements throughout the product lifecycle.
• Collaborate with R&D, Engineering, and Manufacturing to ensure quality is designed into new products and processes.
• Lead risk management activities, including FMEA and hazard analysis.
• Oversee validation and verification activities for products and processes.
• Manage supplier quality programs and conduct supplier audits.
• Drive continuous improvement initiatives to enhance product quality and process efficiency.

• Bachelor's or Master's degree in a scientific, engineering, or related field.
• Minimum of 7 years of experience in Quality Assurance within the medical device industry.
• In-depth knowledge of ISO 13485, FDA regulations (21 CFR Part 820), and other relevant international standards.
• Proven experience in developing, implementing, and maintaining a QMS.
• Strong leadership, team management, and people development skills.
• Experience with CAPA, change control, and document control systems.
• Proficiency in risk management techniques (e.g., FMEA).
• Experience with audits and regulatory inspections.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong written and verbal communication skills, with the ability to interact effectively with all levels of the organization and external stakeholders.
• Certification such as ASQ CQE or equivalent is highly desirable.

The role of the Quality Control is to ensure that our product is always acceptable and meets the correct, Specification as well as promoting the benefits of high standards of Product Quality. Quality Control will aid the efficiency of the business by ensuring that the product is right first time.  This role includes taking product samples and supporting the wider quality/ technical team.

Your main accountabilities will be to:

• Measure quality assurance at production level against confirmed specifications
• Work alongside Production Operatives to ensure quality is a pivotal part of daily tasks
• Complete and be accountable for accurate Quality and Due Diligence records
• Escalate quality or food safety concerns immediately to the appropriate level.
• Ensure that the correct product is packed
• Support the quality auditing process
• Take samples during and after production and carry out quality testing.

Shift pattern 4 days x 12 hours week 1, 4 nights x 12 hours week 2. 7am to 7pm or 7pm to 7am.

Requirements

• Experience in a retail/food manufacturing environment.
• Experience in quality assurance/quality control/ food safety/ environmental standards/ organics.
• Knowledge of Microsoft Office.

• Working experience within a similar role and/or a food environment.
• Awareness of the importance of food safety

Benefits

Some of our benefits include:

• Competitive Salary
• NEST Pension Scheme
• Annual Leave – 24.8 days
• Long service awards
• Employee Wellness Programmes
• Life Assurance
• Ride to Work Scheme

Quality Control Technologist/QC - Thermoplastic Coatings - Milton Keynes

Our client manufactures high quality road marking materials for the Highway Construction and Maintenance sector offering specialist installation of a range of road marking materials and surface treatment products. They also provide full technical support including in-situ testing and monitoring for inter-company divisions and their clients.

An opportunity has arisen for a self-motivated individual to primarily undertake Quality Control (QC) testing in their well-equipped laboratories based at their site in Buckinghamshire.

Responsibilities:

• Report to the Laboratory and Development Manager
• Quality Control (QC) testing of production samples and key raw materials.
• Support to manufacturing e.g., Non-conformance Reports (NCRs).
• Assistance with customer complaints investigations.
• Assistance with calibration of equipment.
• Ensuring all tasks are undertaken safely and in a timely manner.
• Maintaining good housekeeping and tidying of the laboratory.
• Assistance with raw material evaluations, product improvement and development.

Candidate Profile:

• Preferably qualified to a minimum of A level in chemistry and physics or to an equivalent standard, you will possess sound technical aptitude and analytical skills gained from your previous experience.
• Well organised and methodical but with a creative and flexible approach.
• Must be computer literate with excellent verbal and written skills and be comfortable working on your own initiative as well as part of a team.
• A full driving licence is a mandatory requirement as some external site visits and testing will be required.

Whitehall is the Recruitment Specialist for the Chemical, Polymer, Coatings and Life Science Industries.

We are recruiting for a Quality Control Manager to join an established Manufacturing business based in the Dudley area. The Quality Control Manager will be working within a busy Quality department where you will be responsible for ensuring products meet Quality standards and working to improve operational efficiency.

As the Quality Control Manager you will be required too :

• Developing and implementing QMS systems, ensuring that quality standards and regulations are met
• Support and manage a CRM system to track projects and new developments
• Work on projects to support the optimisation of energy meeting objectives for sustainable manufacturing
• Oversee the inspection & testing of materials, goods & products to identify any possible defects
• Managing a team of Quality control inspectors ensuring an effective quality control process
• Support concepts and improvements in inspection
• Carrying out audits & maintaining Quality Assurance
• Liaising with other departments to address Quality issues and implement corrective actions where necessary
• Ensuring compliance with industry standards working to industry standards and regulations

Requirements:

• Experienced in a Quality Control/Management position
• Familiar with quality operations PPAP/APQP or equivalent
• Experienced working to ISO 9001
• Able to drive Change and Improvement
• Able to implement best practice solutions
• Experienced in Manufacturing, Automotive or foundry environments

If you would be interested in the position of Quality Control Manager please apply now and we will be in touch shortly.

Quality Control Engineer - East Sussex - 35k

Platform Recruitment has partnered with amanufacturing leader to find a Quality Control Engineer at their East Sussex site.

This role willensure products meet internal and customer quality standards, leading inspections, audits, and problem-solving initiatives. You'll collaborate across production, suppliers, and customers to drive quality improvements.

Key Responsibilities

• Investigate and resolve non-conformances

• Inspect electronic/mechanical parts and assemblies

• Conduct audits and support supplier quality activities

• Apply 8D and root cause analysis methods

About You

• Qualification in Electronics

• Strong knowledge of ISO9001/ISO14001

• Skilled in inspection of PCBs, wiring, assemblies

• Able to read CAD drawings, BOMs, and technical documentation.

If you feel like you have the right skills and experience for this role, then please apply with a copy of your updated CV.

Quality Control Inspector (Temp to Perm)
Location: Sandwich | Department: Quality

We're looking for a Quality Control Inspector to join our clients team on a temp to perm basis . You'll be inspecting electrical, electronic, optical and mechanical parts, keeping accurate records, and helping resolve any defects.

What you'll do:

• Inspect incoming parts, sub-assemblies and finished products
• Record and report defects, quarantine faulty items
• Use measuring tools (verniers, micrometres, gauges) to check tolerances
• Calibrate and maintain inspection equipment
• Support continuous improvement and quality standards

What we're looking for:

• Experience in an engineering/machine shop environment
• Strong attention to detail and able to read engineering drawings
• Confident with inspection tools; CMM experience is a plus
• Good knowledge of electro-mechanical equipment
• Reliable, motivated and able to work with minimal supervision

You will be working a 9 day fortnight so will have alternative Fridays off and the hours are 8.00am - 4.45pm Monday to Thursday and 8.00am - 4.30pm Fridays.

This is initially a temporary role, however for the right person there could be the opportunity to become permanent.

New Appointments Group, Expertly Matching Employers and Jobseekers since 1975.

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