Latest Medical Imaging Jobs

Senior Customer Training Specialist – Hugo RAS Technology

This role involves delivering high-level technical training and support for the Medtronic Hugo RAS robot, covering surgical indications in General Surgery, Urology, and Gynaecology. You will train surgeons, first assistants, and OR staff, apply structured teaching methodologies, and collaborate with sales and clinical teams to ensure the success of robotic surgery programs.

Medtronic £58,400 – £87,600 pa

Hybrid Permanent

Technical Consultant (Aortic, Neurovascular, Peripheral Vascular) - Khobar

This role involves providing clinical and technical support during vascular procedures, educating healthcare professionals on Medtronic's technologies, and collaborating with the sales and marketing teams to drive therapy adoption. The Technical Consultant will work in a field-based capacity, primarily in the Eastern Region of Saudi Arabia, with regular travel and a home-office setup.

Medtronic Saudi Arabia

Hybrid Permanent

Contract Excellence Lead - International

Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We are looking for a Contract Excellence Lead for our International region to join our Commercial Centre of Excellence. In this influential role, you will shape...

Smith & Nephew Birmingham, United Kingdom

Manager, Safety Analysis Scientist

The Manager, Safety Analysis Scientist role involves leading the safety assessment of assigned products, preparing scientific safety analyses, and collaborating with cross-functional teams to ensure regulatory compliance. The role requires in-depth product knowledge, mentoring team members, and supporting safety management teams.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Associate Director, Safety Analysis Scientist

This role involves leading scientific safety evaluations for pharmaceutical products across development and post-marketing stages, with a focus on analyzing complex medical data, shaping safety strategies, and supporting regulatory compliance. The scientist will serve as a subject matter expert, lead cross-functional safety reviews, contribute to key clinical documents, and drive innovation in safety analysis methodologies. Emphasis is placed on proactive risk assessment, collaboration with global teams, and ensuring high-quality, timely safety reporting.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Director, Clinical Risk Management Post Approval Delivery Unit

This role involves overseeing clinical risk management for post-approval clinical trials, ensuring data integrity, patient safety, and compliance with regulatory requirements. Responsibilities include leading a team of CRM Representatives, conducting risk assessments, and developing mitigation strategies.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Associate Director, Regulatory Policy

The Associate Director, Regulatory Policy, provides leadership in regulatory compliance and policy, ensuring alignment with global and regional requirements. Key responsibilities include interpreting regulatory policies, developing internal guidelines, and supporting cross-functional teams to manage regulatory risks and enable informed decision-making.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular review cycles.

Johnson & Johnson MedTech United States

On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include active participation in study activities, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech

On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and communicating risk updates to stakeholders through regular review cycles.

Johnson & Johnson MedTech

On-site Permanent

Director, 3rd Party RM. Program (BPO)

The Director, 3rd Party RM Program (BPO) leads the development and implementation of a global third-party risk management program, focusing on anti-bribery and anti-corruption. Key responsibilities include strategic governance, risk assessment, due diligence, and technology integration to ensure compliance and sustainable growth.

Johnson & Johnson MedTech

On-site Permanent

Specialist, Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium

On-site Permanent

Biosurgery Sales Specialist| J&J MedTech | Surgery | East Midlands

This role involves driving sales growth for Johnson & Johnson MedTech's biosurgery (haemostats) portfolio in the East Midlands, focusing on key surgical centres. The specialist will develop and execute account strategies, build relationships with surgeons and healthcare professionals, and collaborate across J&J teams to expand adoption of wound closure technologies in both NHS and private sectors.

Johnson & Johnson MedTech United Kingdom

Hybrid Permanent

Senior Scientist Clinical Pharmacokinetics

The Senior Scientist Clinical Pharmacokinetics role involves leading the end-to-end execution of Phase 1 clinical pharmacology studies, including protocol development, data analysis, and report writing. Additional responsibilities include supporting all phases of drug development with noncompartmental analysis and contributing to regulatory submissions.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site 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