Latest quality assurance Jobs

QMS Specialist

As a QMS Specialist, you will ensure the Quality Management System meets global medical device regulations, support key QMS processes, and collaborate with cross-functional teams to maintain audit readiness. Your role involves interpreting regulatory requirements, conducting data analysis, and driving continuous improvement to ensure high-quality, compliant products.

Smith & Nephew Goole, United Kingdom

Hybrid Permanent

Philips Holter Technician/Analyst

Analyzes Holter monitor ECG recordings to ensure clinical accuracy and completeness of diagnostic data for physician review. Performs quality assurance on ECG readings, interprets rhythm data against notification criteria, and supports reliable patient reporting. Works within established SOPs while maintaining meticulous attention to detail in a regulated healthcare environment.

Philips Rushmoor, GU14 7JT, United Kingdom

On-site Temporary

Philips Holter Technician/Analyst

Analyze Holter ECG recordings to ensure clinical accuracy and support physicians with reliable diagnostic data. Focus on quality assurance, rhythm interpretation, and adherence to SOPs while contributing to patient care. Work both independently and collaboratively within a structured office environment.

Philips

On-site Temporary

Manufacturing Engineer

This role involves designing and refining high-precision manufacturing processes for patient-specific medical devices, with a focus on scalability and repeatability. The engineer will optimise 5-axis CNC and CAM workflows, implement rigorous quality systems, and drive continuous improvement in a tightly controlled production environment. The position plays a key role in shaping a globally scalable manufacturing operation with future international expansion in mind.

Reed Wa37Gb, United Kingdom £50,000 – £90,000 pa

On-site Permanent

Senior QA Validation Engineer

This role involves leading software verification and validation for safety-critical systems in a regulated environment, with a focus on test automation, regulatory compliance, and end-to-end traceability. The engineer will design test strategies, develop automated frameworks, and ensure alignment with quality standards across the development lifecycle. Collaboration with cross-functional teams is essential to resolve quality issues and support audits or regulatory submissions.

SoCode Impington, Cambridgeshire, United Kingdom £80,000 – £100,000 pa

On-site Permanent

Electronics Engineer Consultant - Security Clearance

Electronics Engineer Consultant - Security Clearance - CambridgeA new design consultancy, based in Cambridge, are currently looking for a Electronics Engineer Consultant to add to the team of experienced experts, specifically with a focus on security cleared projects.Although this is...

Newton Colmore Cambridge, United Kingdom

Process Engineer, Validation

The Process Engineer, Validation leads and executes validation activities for new product ranges and changes to existing medical devices. They ensure all manufacturing processes, equipment, and test methods meet internal and external regulatory standards, working closely with cross-functional teams and external partners. The role involves developing validation strategies, authoring protocols, conducting risk assessments, and supporting regulatory submissions.

OrganOx Oxford, United Kingdom

On-site Permanent

Mechanical Engineer - Genomics Instrumentation - Cambridge

You will work within a multidisciplinary team to design and develop cutting-edge genomics instrumentation, contributing to high-throughput genomic workflows and precision diagnostics. Your role involves the full product lifecycle, from concept development to product launch.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Senior I Stat Prog Lead

This role involves leading statistical programming activities for clinical projects, developing programming strategies, and delivering high-quality data analysis and reporting. The Senior Statistical Programming Lead provides technical guidance to teams, ensures compliance with data standards and SOPs, and contributes to submissions and cross-functional initiatives. It emphasizes advanced SAS programming, clinical trial data structures, and collaboration within a regulated environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

CQ Lead and RP Surgery UK/Ireland

This role involves leading the quality management framework and system for Johnson & Johnson's Surgery division in the UK and Ireland. Responsibilities include managing quality systems, ensuring compliance, leading regional projects, and integrating quality management across multiple markets. The position requires strategic leadership and interaction with global projects and regulatory bodies.

Johnson & Johnson MedTech United Kingdom

On-site Permanent

Tech Transfer Engineer

ABOUT ORGANOX:OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and...

OrganOx Oxford, United Kingdom

On-site

Quality Officer

You will support the Quality function in maintaining and improving the Quality Management System (QMS), ensuring ongoing compliance with GDP standards, ISO requirements, and client expectations. This is a key role focused on driving quality administration efficiency, supporting audits, and...

Robert Walters Derbyshire, United Kingdom £40,000 – £42,000 pa

Quality Engineer

As a Quality Engineer, you will drive quality excellence in a regulated manufacturing environment, leading improvement initiatives, compliance efforts, and problem-solving. You will collaborate with cross-functional teams to ensure product quality, process performance, and regulatory compliance, using structured methodologies and statistical analysis.

Consortium Professional Recruitment Hessle, East Riding Of Yorkshire, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Quality Engineer

As a Quality Engineer, you will lead quality initiatives in a manufacturing environment, ensuring the reliability and compliance of medical devices. You will apply statistical process control, conduct root cause analysis, and collaborate with cross-functional teams to drive continuous improvement and maintain quality standards.

Smith & Nephew Goole, United Kingdom

On-site Permanent

Design Engineer (Medical Devices / SolidWorks)

This role involves designing medical devices from concept to production, using SolidWorks to create 3D models and detailed drawings. The engineer will support prototyping, testing, and regulatory compliance while collaborating with manufacturing and cross-functional teams. The work contributes to life-changing healthcare products used globally.

Ernest Gordon Recruitment Lisburn, County Antrim, United Kingdom £45,000 – £50,000 pa

Hybrid Permanent