Medical Technology Jobs

Johnson & Johnson MedTech · Raritan, United States · US$102,000 – US$177,100 pa

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors performing anonymisation and synthetisation, serves as the primary contact for YODA Project requests, and supports external research teams using clinical study data. Operates independently as a subject matter expert within the Clinical Data Standards and Transparency team.

Johnson & Johnson MedTech · High Wycombe

Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection/submission readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving quality risk monitoring reviews, supporting CAPA plans, and leading inspection readiness and mock inspections with cross-functional teams.

Smith & Nephew · Hull

Leads strategic initiatives to shape and continuously improve a global compliance programme, simplifying processes, enhancing systems and overseeing reporting, communications and training roadmaps. Works cross-functionally with Compliance, Finance and People teams, measuring programme effectiveness and supporting leadership reporting.

Smith & Nephew · Hull

Acts as a key technical resource supporting manufacturing operations through automation, controls and machine connectivity solutions. Drives Smart Factory capabilities, resolves production issues and promotes cybersecurity best practices across OT systems at multiple sites, liaising between the OT Centre of Excellence and plant operations.

Medtronic · Heerlen, Netherlands · €40,000 – €60,000 pa

Serve as the primary point of contact for customers throughout the service and repair journey, managing requests, quotations, orders and escalations while coordinating with service engineers, repair centers and logistics teams. Support quality and compliance in a regulated MedTech setting and contribute to process improvements, system enhancements and UAT activities.

Medtronic · Heerlen, Netherlands · €50,000 – €75,000 pa

Acts as a subject matter expert handling complex customer inquiries, escalations, quotations and orders while driving process improvements and system enhancements. Supports projects, UAT and training within a newly built in-house Service & Repair Customer Care organisation, working in English and French with healthcare providers.

Clearline Recruitment Ltd · Welwyn Garden City · £38 – £56 ph

Independently manages end-to-end clinical data management across one or more studies, from CRF and database design through to final study closure. Works closely with Biostatistics, Data Science and Clinical Operations, overseeing data vendors and resolving complex issues across EDC, ePRO and IRT systems. Requires strong knowledge of CDISC standards and risk-based monitoring.

Reed Technology · Cambridge · £85,000 – £100,000 pa

Lead information security, product cybersecurity and cyber risk management for a digital health organisation, owning the ISMS, policies and controls. Day to day involves risk assessments, threat modelling, penetration testing oversight, cloud and application security, incident response and supporting audits and regulatory submissions. Works closely with software development, quality, regulatory and clinical teams, acting as the security subject matter expert.

Evolve Selection · Hemel Hempstead

Leads the UK Medical Affairs strategy for an aesthetics organisation, developing integrated brand medical plans and feeding medical insight into a three-year business strategy. Drives evidence generation, publication planning, real-world evidence and KOL engagement while building scientific capability across Commercial and Marketing. Manages a multidisciplinary Medical Affairs team and reports to the Country Manager.

Clearline Recruitment Ltd · Welwyn Garden City · £377 – £550 pd

Operational delivery of early-phase clinical trials, coordinating multi-country study activities, timelines and site start-up while managing vendors, CROs and study documentation such as Trial Master Files. Works closely with international study teams and cross-functional groups to ensure ICH-GCP compliance, manage risks and improve study processes.

Platform Recruitment · Royston · £45,000 – £50,000 pa

Develops high-quality, well-documented embedded software in C/C++ on RTOS or bare metal, working across the full lifecycle from requirements capture to verification and release. Sits in multi-disciplinary teams with client-facing communication and significant ownership of design decisions on medical devices.

Computer Futures · London · £75,000 – £85,000 pa

Drive software safety activities across the product lifecycle for software-based medical devices, including hazard analysis, risk assessments and safety documentation. Work with Software, Quality, Regulatory and Product Development teams to ensure compliance with standards such as ISO 14971 and IEC 62304, and support verification, validation and software risk management.

Talentmark · Wrexham · £22 – £29 ph

Translate business requirements into user stories and acceptance criteria, working with a scrum master on story sizing and risk analysis. Participate in release and sprint planning, backlog grooming and sprint reviews, collaborating with software engineers, QA and dev-ops. Focused on clinical trial software such as EDC or eCOA within a 21 CFR Part 11 regulated environment.

Wallace Hind Selection · Watford · £35,000 – £40,000 pa

Consultative field sales role promoting vascular access and oncology medical devices to NHS and private healthcare customers across the M25 region, with 80% new business generation and 20% account development. Involves theatre-based demonstrations, quotations, and attending congresses, with full training and mentoring provided.

Wallace Hind Selection · Sevenoaks · £35,000 – £40,000 pa

Consultative field sales role promoting vascular access and oncology medical devices to NHS and private healthcare customers across the M25 region. Roughly 80% new business generation and 20% account development, including quotations, equipment demonstrations, and attendance at fairs and congresses, with full training and mentoring provided.