Medical Technology Jobs

Medical Safety Officer - Solid Tumors

The Medical Safety Officer (MSO) is responsible for assessing the medical safety of Innovative Medicine products and leading cross-functional teams in safety and benefit risk management. Key responsibilities include safety surveillance, risk management, and communication with stakeholders, including Health Authorities and external key opinion leaders.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Distribution & Transportation Senior Supervisor (m/f/d)

Oversee distribution and transportation operations for MedTech products, ensuring compliance, cost efficiency, and on-time delivery to patients. Lead third-party logistics partners, drive process improvements using data analytics, and support new product launches within a regulated GxP environment. Role involves cross-functional collaboration and incident resolution across the EMEA supply chain.

Johnson & Johnson MedTech High Wycombe, United Kingdom £49,300 – £79,695 pa

Service - Field Service Engineer (FSE) – Surgery / X-Ray (XR) - London

Perform planned maintenance, fault diagnosis, and repairs on surgery and X-ray imaging systems across London and surrounding areas. Support installations, upgrades, and out-of-hours service using remote connectivity and on-site troubleshooting. Work independently with a company vehicle to ensure high equipment uptime and strong customer relationships in clinical environments.

GE HealthCare Chalfont St Giles, Buckinghamshire, United Kingdom

Hybrid Permanent Clearance Required

Director, Regulatory Affairs, Europe

Leads the European Regulatory Affairs team at GE HealthCare, defining regulatory strategy and ensuring compliance with EU MDR and UK MDR for medical devices. Oversees CE and UKCA marking, manages interactions with Notified Bodies and Competent Authorities, and drives regulatory alignment across quality, legal, and product teams. Focuses on strategic planning, postmarket compliance, and industry engagement in a global healthcare technology environment.

GE HealthCare Chalfont St Giles, Buckinghamshire, United Kingdom

Medical Safety Officer - PALM

This role involves leading the medical safety assessment of pharmaceutical products in clinical development and post-approval, with a focus on signal detection, risk management, and regulatory compliance. The Medical Safety Officer provides strategic medical input into safety documentation, collaborates across clinical and regulatory teams, and ensures accurate communication of safety data to internal stakeholders and health authorities. The position plays a key role in shaping risk mitigation strategies and maintaining compliance with global pharmacovigilance standards.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Experienced I Stat Programmer

This role involves designing and developing statistical programs for clinical research analysis, with a focus on high-quality, timely deliverables. The programmer will verify code, maintain documentation, and collaborate with cross-functional teams to support clinical trial reporting. Emphasis is placed on compliance, data quality, and improving programming efficiency within a regulated environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Senior I Stat Prog Lead

Leads statistical programming activities for clinical projects, ensuring high-quality, timely deliverables in compliance with regulatory standards. Designs and develops programs for complex clinical data analysis, provides technical guidance to teams, and contributes to process improvements. Works closely with cross-functional teams to support clinical trial reporting and submissions.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Experienced I Clin Programmer

Develops and oversees clinical data programming for complex trials, creating CDISC-compliant SDTM datasets and define.xml, implementing data mappings, edit checks, and custom safety/compliance reports. Focuses on data quality, regulatory standards, and integration of diverse clinical data sources to support trial oversight and submissions.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Associate Director, Clinical Risk Management

This role involves leading clinical risk management across multiple therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The individual will drive risk-based monitoring, support inspection readiness, lead quality investigations, and provide strategic guidance on CAPA and regulatory standards within a global, cross-functional R&D environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Director, Regulatory Data Office Leader

This role involves leading a global team of data stewards and overseeing the Regulatory Data Hub to ensure high-quality regulatory data for business intelligence and decision-making. The Director will establish data governance policies, collaborate across R&D and IT, and drive regulatory data transformation initiatives.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Digital Adoption and Sales Specialist UK&I + Nordics– RO - MIM Software

Drives adoption of digital solutions in Radiation Oncology and Molecular Imaging by leading product demonstrations, managing trials, and ensuring successful customer integration. Acts as a key liaison between clinical users, sales teams, and product development to enhance value realization and support long-term engagement. Focuses on customer success, training alignment, and commercial growth through data-driven engagement strategies.

GE HealthCare Chalfont St Giles, Buckinghamshire, United Kingdom £50,000 pa