Latest Medical Imaging Jobs

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation. Key responsibilities include stakeholder engagement, evidence generation, and supporting regulatory and market access initiatives. The role involves deep engagement with the healthcare ecosystem to identify unmet needs and translate them into actionable insights.

Johnson & Johnson MedTech Manchester, United Kingdom

On-site Permanent

Medical Governance Manager

This role involves implementing and maintaining the UK medical governance framework, reviewing and certifying materials, and providing compliance training. The position is pivotal in ensuring high ethical standards and compliance with the ABPI Code of Practice, working closely with cross-functional teams.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Head of QARA

Cure Talent are delighted to be partnered with an innovative medical technology company transforming access to ear and hearing healthcare. Operating at the intersection of medical devices and software, the business is scaling its global presence and is now looking...

Cure Talent Marylebone High Street, London, United Kingdom £80,000 – £90,000 pa

On-site Permanent

Regulatory Affairs Manager

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...

Cure Talent Curbridge, Oxfordshire, United Kingdom

International Repairs Administrator

Process repair orders for a global customer base, manage inbound documentation, quotations, and shipping logistics while serving as the primary point of contact for overseas customers. Support sales administration and contribute to process improvements within a high-growth medical devices company.

Enterprise Recruitment Aston Clinton, Buckinghamshire, United Kingdom £28,000 – £30,000 pa

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

Technical Documentation and Development Engineer

A Technical Documentation & Development Engineer is required to support medical device product development through robust documentation, CAD formalisation, and regulatory compliance. The role focuses on ensuring all new and legacy products meet MDR requirements, with a strong emphasis on...

Michael Page Sheffield, South Yorkshire, United Kingdom

Regulatory Affairs Specialist

As a Regulatory Affairs Specialist, you will work within a global team to ensure medical devices meet regulatory requirements. Your responsibilities include preparing regulatory submissions, collaborating with project teams, and maintaining compliance throughout the product lifecycle.

Smith & Nephew Watford, United Kingdom

Hybrid 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

Control Systems Engineer

The Control Systems Engineer will develop and implement software for complex automation and robotic systems, commission and test machinery, diagnose faults, and support installations at customer sites. The role involves programming industrial robots, conducting machine testing, ensuring compliance with safety standards, and providing customer training and support.

Automation Experts Ltd Leicester, Leicestershire, United Kingdom £45,000 – £65,000 pa

On-site Permanent

Senior Analyst

The Senior Analyst role involves developing and refining pharmaceutical business fundamentals databases, supporting product and client needs, and collaborating with local and offshore teams. Responsibilities include data collection, quality control, and enhancing database accuracy and scope.

GlobalData Plc Blackfriars, City And County Of the City Of London, EC4V 6BJ, United Kingdom

Hybrid Permanent

Scientist

The Scientist role involves reviewing clinical data, writing technical reports, and ensuring medical devices meet regulatory requirements for CE marking and global approval. You will collaborate with a scientific and clinical team, prepare high-quality reports, and manage changing priorities in a fast-paced environment.

Peopleforce Recruitment Ltd Witney, Oxfordshire, United Kingdom £23 ph

On-site Permanent

Computational Physicist - AI for Healthcare

This role involves leading research in AI-driven healthcare technology, applying computational physics expertise to develop novel algorithms and tools using machine learning and advanced sensors. The candidate will act as the subject matter expert in physical sciences, guiding R&D efforts and contributing to the evolution of medical device technology. Work takes place in state-of-the-art labs with a focus on solving complex scientific and engineering challenges.

Newton Colmore London, United Kingdom

Hybrid Permanent

Production Scheduler

The Production Scheduler will plan, coordinate, and monitor production activities across multiple projects in a regulated medical device manufacturing environment. Key responsibilities include developing realistic schedules, working closely with cross-functional teams, and supporting continuous improvement initiatives.

Euro Projects Recruitment Abingdon, Oxfordshire, OX14 5BH, United Kingdom £40,000 – £45,000 pa

On-site Permanent

CAD Design Engineer

The CAD Design Engineer will be responsible for the product design and development of medical devices from concept to market release. Key tasks include creating 3D models, managing design changes, and ensuring compliance with engineering standards. The role offers on-the-job training and opportunities for career progression within a rapidly expanding, globally recognized medical device company.

Hunter Selection Aberdare, Mid Glamorgan, United Kingdom £30,000 – £36,000 pa

On-site Permanent