Latest quality assurance Jobs

Quality Assurance & Regulatory Affairs Specialist - MedTech

This role involves ensuring quality assurance and regulatory compliance across the full lifecycle of advanced medical devices, from design through manufacturing, for global markets including Europe, North America, and APAC. The specialist will conduct internal audits, help shape regulatory strategy, and work with complex, innovative technologies in a high-autonomy environment. The role focuses on new product development, requiring strict adherence to ISO 13485, CE Marking, and other international standards.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £45,000 – £49,000 pa

On-site Permanent

Quality Assurance Specialist

This role involves maintaining and improving the company's Quality Management System (QMS) within a regulated Medical Device manufacturing environment. Responsibilities include ISO13485 compliance, internal auditing, CAPA management, complaint investigations, and regulatory support. The position is office-based and requires strong documentation and procedural writing skills.

East Lancashire Services Crimble, Manchester, OL11 4AB, United Kingdom

On-site Permanent

Test Quality Assurance Engineer

This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Quality Engineer

The Quality Engineer will lead root cause investigations, drive corrective actions, and support new product introductions in a regulated manufacturing environment. They will work closely with cross-functional teams to ensure quality compliance and continuous improvement.

Owen Daniels Coventry, United Kingdom £40,000 – £45,000 pa

On-site Permanent

Quality and Regulatory Labelling Program Manager

This role involves leading global labelling initiatives to ensure compliance with regulatory standards across various markets. The Program Manager will collaborate with cross-functional teams to manage change controls, mitigate risks, and drive continuous improvement in labelling processes.

Randstad Engineering Popley, Hampshire, RG24 9TW, United Kingdom £27 ph

Hybrid Contract

Quality Control Release Specialist 2

This role involves ensuring compliance with regulatory requirements and company procedures for the release of manufactured medical products. Responsibilities include leading the coordination and training of QC Release personnel, managing quality processes, and supporting continuous improvement initiatives.

Smith & Nephew Goole, United Kingdom

On-site Permanent

Quality & Regulatory Associate

This role involves supporting the Quality Management System (QMS) and Regulatory processes, including ISO13485 readiness and FDA 510(k) documentation. You will work closely with internal teams to maintain quality documentation, manage change controls, and promote continuous improvement.

Taylorollinson Manchester, United Kingdom £35,000 – £45,000 pa

Hybrid Permanent

Software Quality Engineer

The Software Quality Engineer supports software quality assurance by ensuring regulatory compliance in software lifecycle documentation, testing, and adherence to coding standards. They will work closely with R&D, Post-Market Engineering, and Quality teams to manage design and development, risk assessment, and change control processes.

OrganOx Oxford, United Kingdom

On-site Permanent

Senior Supplier Assurance Engineer

The Senior Supplier Assurance Engineer leads supplier quality activities, ensuring compliance with global regulations and internal QMS processes. Key responsibilities include supplier qualification, performance monitoring, and continuous improvement, with a focus on maintaining high-quality standards across the supply chain.

OrganOx Oxford, United Kingdom

On-site Permanent Flexible

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

QC Manager

Lead and manage the day-to-day operations of a QC laboratory within a regulated personal care and skincare manufacturing environment. Oversee analytical testing, root cause investigations, and ensure compliance with GMP, ISO, and GDP standards. Develop laboratory staff and drive continuous improvement in quality and performance.

SRG Po92Ax, PO9 2AX, United Kingdom

On-site Permanent

Regulatory Affairs Specialist - Medical Devices

This role involves leading quality assurance and regulatory affairs initiatives for medical devices within a global R&D and manufacturing environment. You'll work across European, American, and Asian regulatory standards, driving compliance and developing innovative solutions for quality systems. The position offers exposure to highly regulated industries and complex international projects.

Newton Colmore Cambridge, United Kingdom £42,000 – £46,000 pa

On-site Permanent

QC Technician

The QC Technician will perform quality control inspections, test materials and finished products, maintain accurate records, and support the Quality Assurance team to ensure compliance with GMP standards. The role involves working in a busy manufacturing environment, maintaining high levels of accuracy and attention to detail.

Winsearch Shotwick, Cheshire, CH1 6HZ, United Kingdom £13 ph

On-site Temporary

QC Release Specialist 2

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Smith+Nephew is hiringQC Release Specialist 2 .The Quality Compliance release team is focused on ensuring that Smith + Nephew complies with key regulatory requirements and Smith...

Smith & Nephew Goole, United Kingdom

Philips Holter Technician/Analyst

The role involves analyzing Holter ECG recordings to ensure clinical accuracy and completeness, supporting physicians with reliable diagnostic data. The technician ensures quality assurance in ECG readings, adheres to SOPs, and maintains high attention to detail while interpreting cardiac rhythms. Ongoing development in ECG interpretation and collaboration within a clinical team are key aspects of the position.

Philips Hastings, TN38 8AJ, United Kingdom

On-site Temporary